MedPath

Amlodipine and atorvastatin

AMLODIPINE AND ATORVASTATIN Tablets

Approved
Approval ID

337b47f6-d4df-48ed-b19f-96fcbae3884b

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Oct 13, 2022

Manufacturers
FDA

Zydus Lifesciences Limited

DUNS: 918596198

Products 10

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Amlodipine and atorvastatin

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code70771-1459
Application NumberANDA207762
Product Classification
M
Marketing Category
C73584
G
Generic Name
Amlodipine and atorvastatin
Product Specifications
Route of AdministrationORAL
Effective DateOctober 13, 2022
FDA Product Classification

INGREDIENTS (13)

AMLODIPINE BESYLATEActive
Quantity: 2.5 mg in 1 1
Code: 864V2Q084H
Classification: ACTIM
CALCIUM CARBONATEInactive
Code: H0G9379FGK
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
CROSCARMELLOSE SODIUMInactive
Code: M28OL1HH48
Classification: IACT
HYDROXYPROPYL CELLULOSE, UNSPECIFIEDInactive
Code: 9XZ8H6N6OH
Classification: IACT
HYPROMELLOSESInactive
Code: 3NXW29V3WO
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
POLYSORBATE 80Inactive
Code: 6OZP39ZG8H
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
TALCInactive
Code: 7SEV7J4R1U
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
ATORVASTATIN CALCIUM TRIHYDRATEActive
Quantity: 40 mg in 1 1
Code: 48A5M73Z4Q
Classification: ACTIM

Amlodipine and atorvastatin

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code70771-1458
Application NumberANDA207762
Product Classification
M
Marketing Category
C73584
G
Generic Name
Amlodipine and atorvastatin
Product Specifications
Route of AdministrationORAL
Effective DateOctober 13, 2022
FDA Product Classification

INGREDIENTS (13)

AMLODIPINE BESYLATEActive
Quantity: 2.5 mg in 1 1
Code: 864V2Q084H
Classification: ACTIM
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
HYPROMELLOSESInactive
Code: 3NXW29V3WO
Classification: IACT
CALCIUM CARBONATEInactive
Code: H0G9379FGK
Classification: IACT
CROSCARMELLOSE SODIUMInactive
Code: M28OL1HH48
Classification: IACT
HYDROXYPROPYL CELLULOSE, UNSPECIFIEDInactive
Code: 9XZ8H6N6OH
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
POLYSORBATE 80Inactive
Code: 6OZP39ZG8H
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
TALCInactive
Code: 7SEV7J4R1U
Classification: IACT
ATORVASTATIN CALCIUM TRIHYDRATEActive
Quantity: 20 mg in 1 1
Code: 48A5M73Z4Q
Classification: ACTIM

Amlodipine and atorvastatin

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code70771-1463
Application NumberANDA207762
Product Classification
M
Marketing Category
C73584
G
Generic Name
Amlodipine and atorvastatin
Product Specifications
Route of AdministrationORAL
Effective DateOctober 13, 2022
FDA Product Classification

INGREDIENTS (13)

CALCIUM CARBONATEInactive
Code: H0G9379FGK
Classification: IACT
AMLODIPINE BESYLATEActive
Quantity: 5 mg in 1 1
Code: 864V2Q084H
Classification: ACTIM
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
CROSCARMELLOSE SODIUMInactive
Code: M28OL1HH48
Classification: IACT
HYDROXYPROPYL CELLULOSE, UNSPECIFIEDInactive
Code: 9XZ8H6N6OH
Classification: IACT
HYPROMELLOSESInactive
Code: 3NXW29V3WO
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
POLYSORBATE 80Inactive
Code: 6OZP39ZG8H
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
TALCInactive
Code: 7SEV7J4R1U
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
ATORVASTATIN CALCIUM TRIHYDRATEActive
Quantity: 80 mg in 1 1
Code: 48A5M73Z4Q
Classification: ACTIM

Amlodipine and atorvastatin

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code70771-1457
Application NumberANDA207762
Product Classification
M
Marketing Category
C73584
G
Generic Name
Amlodipine and atorvastatin
Product Specifications
Route of AdministrationORAL
Effective DateOctober 13, 2022
FDA Product Classification

INGREDIENTS (13)

AMLODIPINE BESYLATEActive
Quantity: 2.5 mg in 1 1
Code: 864V2Q084H
Classification: ACTIM
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
HYDROXYPROPYL CELLULOSE, UNSPECIFIEDInactive
Code: 9XZ8H6N6OH
Classification: IACT
HYPROMELLOSESInactive
Code: 3NXW29V3WO
Classification: IACT
POLYSORBATE 80Inactive
Code: 6OZP39ZG8H
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
TALCInactive
Code: 7SEV7J4R1U
Classification: IACT
CALCIUM CARBONATEInactive
Code: H0G9379FGK
Classification: IACT
CROSCARMELLOSE SODIUMInactive
Code: M28OL1HH48
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
ATORVASTATIN CALCIUM TRIHYDRATEActive
Quantity: 10 mg in 1 1
Code: 48A5M73Z4Q
Classification: ACTIM

Amlodipine and atorvastatin

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code70771-1461
Application NumberANDA207762
Product Classification
M
Marketing Category
C73584
G
Generic Name
Amlodipine and atorvastatin
Product Specifications
Route of AdministrationORAL
Effective DateOctober 13, 2022
FDA Product Classification

INGREDIENTS (13)

AMLODIPINE BESYLATEActive
Quantity: 5 mg in 1 1
Code: 864V2Q084H
Classification: ACTIM
HYDROXYPROPYL CELLULOSE, UNSPECIFIEDInactive
Code: 9XZ8H6N6OH
Classification: IACT
CALCIUM CARBONATEInactive
Code: H0G9379FGK
Classification: IACT
CROSCARMELLOSE SODIUMInactive
Code: M28OL1HH48
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
HYPROMELLOSESInactive
Code: 3NXW29V3WO
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
POLYSORBATE 80Inactive
Code: 6OZP39ZG8H
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
TALCInactive
Code: 7SEV7J4R1U
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
ATORVASTATIN CALCIUM TRIHYDRATEActive
Quantity: 20 mg in 1 1
Code: 48A5M73Z4Q
Classification: ACTIM

Amlodipine and atorvastatin

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code70771-1462
Application NumberANDA207762
Product Classification
M
Marketing Category
C73584
G
Generic Name
Amlodipine and atorvastatin
Product Specifications
Route of AdministrationORAL
Effective DateOctober 13, 2022
FDA Product Classification

INGREDIENTS (13)

AMLODIPINE BESYLATEActive
Quantity: 5 mg in 1 1
Code: 864V2Q084H
Classification: ACTIM
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
CALCIUM CARBONATEInactive
Code: H0G9379FGK
Classification: IACT
CROSCARMELLOSE SODIUMInactive
Code: M28OL1HH48
Classification: IACT
POLYSORBATE 80Inactive
Code: 6OZP39ZG8H
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
HYPROMELLOSESInactive
Code: 3NXW29V3WO
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
TALCInactive
Code: 7SEV7J4R1U
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
HYDROXYPROPYL CELLULOSE, UNSPECIFIEDInactive
Code: 9XZ8H6N6OH
Classification: IACT
ATORVASTATIN CALCIUM TRIHYDRATEActive
Quantity: 40 mg in 1 1
Code: 48A5M73Z4Q
Classification: ACTIM

Amlodipine and atorvastatin

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code70771-1465
Application NumberANDA207762
Product Classification
M
Marketing Category
C73584
G
Generic Name
Amlodipine and atorvastatin
Product Specifications
Route of AdministrationORAL
Effective DateOctober 13, 2022
FDA Product Classification

INGREDIENTS (14)

AMLODIPINE BESYLATEActive
Quantity: 10 mg in 1 1
Code: 864V2Q084H
Classification: ACTIM
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
FD&C BLUE NO. 2Inactive
Code: L06K8R7DQK
Classification: IACT
CALCIUM CARBONATEInactive
Code: H0G9379FGK
Classification: IACT
HYDROXYPROPYL CELLULOSE, UNSPECIFIEDInactive
Code: 9XZ8H6N6OH
Classification: IACT
CROSCARMELLOSE SODIUMInactive
Code: M28OL1HH48
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
TALCInactive
Code: 7SEV7J4R1U
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
HYPROMELLOSESInactive
Code: 3NXW29V3WO
Classification: IACT
POLYSORBATE 80Inactive
Code: 6OZP39ZG8H
Classification: IACT
ATORVASTATIN CALCIUM TRIHYDRATEActive
Quantity: 20 mg in 1 1
Code: 48A5M73Z4Q
Classification: ACTIM

Amlodipine and atorvastatin

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code70771-1460
Application NumberANDA207762
Product Classification
M
Marketing Category
C73584
G
Generic Name
Amlodipine and atorvastatin
Product Specifications
Route of AdministrationORAL
Effective DateOctober 13, 2022
FDA Product Classification

INGREDIENTS (13)

CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
AMLODIPINE BESYLATEActive
Quantity: 5 mg in 1 1
Code: 864V2Q084H
Classification: ACTIM
CALCIUM CARBONATEInactive
Code: H0G9379FGK
Classification: IACT
CROSCARMELLOSE SODIUMInactive
Code: M28OL1HH48
Classification: IACT
POLYSORBATE 80Inactive
Code: 6OZP39ZG8H
Classification: IACT
HYDROXYPROPYL CELLULOSE, UNSPECIFIEDInactive
Code: 9XZ8H6N6OH
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
HYPROMELLOSESInactive
Code: 3NXW29V3WO
Classification: IACT
TALCInactive
Code: 7SEV7J4R1U
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
ATORVASTATIN CALCIUM TRIHYDRATEActive
Quantity: 10 mg in 1 1
Code: 48A5M73Z4Q
Classification: ACTIM

Amlodipine and atorvastatin

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code70771-1466
Application NumberANDA207762
Product Classification
M
Marketing Category
C73584
G
Generic Name
Amlodipine and atorvastatin
Product Specifications
Route of AdministrationORAL
Effective DateOctober 13, 2022
FDA Product Classification

INGREDIENTS (14)

AMLODIPINE BESYLATEActive
Quantity: 10 mg in 1 1
Code: 864V2Q084H
Classification: ACTIM
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
CROSCARMELLOSE SODIUMInactive
Code: M28OL1HH48
Classification: IACT
FD&C BLUE NO. 2Inactive
Code: L06K8R7DQK
Classification: IACT
CALCIUM CARBONATEInactive
Code: H0G9379FGK
Classification: IACT
HYPROMELLOSESInactive
Code: 3NXW29V3WO
Classification: IACT
HYDROXYPROPYL CELLULOSE, UNSPECIFIEDInactive
Code: 9XZ8H6N6OH
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
TALCInactive
Code: 7SEV7J4R1U
Classification: IACT
POLYSORBATE 80Inactive
Code: 6OZP39ZG8H
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
ATORVASTATIN CALCIUM TRIHYDRATEActive
Quantity: 40 mg in 1 1
Code: 48A5M73Z4Q
Classification: ACTIM

Amlodipine and atorvastatin

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code70771-1464
Application NumberANDA207762
Product Classification
M
Marketing Category
C73584
G
Generic Name
Amlodipine and atorvastatin
Product Specifications
Route of AdministrationORAL
Effective DateOctober 13, 2022
FDA Product Classification

INGREDIENTS (14)

AMLODIPINE BESYLATEActive
Quantity: 10 mg in 1 1
Code: 864V2Q084H
Classification: ACTIM
CALCIUM CARBONATEInactive
Code: H0G9379FGK
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
FD&C BLUE NO. 2Inactive
Code: L06K8R7DQK
Classification: IACT
CROSCARMELLOSE SODIUMInactive
Code: M28OL1HH48
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
HYDROXYPROPYL CELLULOSE, UNSPECIFIEDInactive
Code: 9XZ8H6N6OH
Classification: IACT
HYPROMELLOSESInactive
Code: 3NXW29V3WO
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
POLYSORBATE 80Inactive
Code: 6OZP39ZG8H
Classification: IACT
TALCInactive
Code: 7SEV7J4R1U
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
ATORVASTATIN CALCIUM TRIHYDRATEActive
Quantity: 10 mg in 1 1
Code: 48A5M73Z4Q
Classification: ACTIM

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.