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ATORVASTATIN CALCIUM

These highlights do not include all the information needed to use CALCIUM TABLETS safely and effectively. See full prescribing information for CALCIUM TABLETS. CALCIUM tablets, for oral administration Initial U.S. Approval: 1996

Approved
Approval ID

685bbc7a-7f7b-4f1f-97e7-bd57072a565c

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jun 7, 2017

Manufacturers
FDA

Cambridge Therapeutics Technologies, LLC

DUNS: 080072003

Products 3

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

ATORVASTATIN CALCIUM

PRODUCT DETAILS

NDC Product Code70882-119
Application NumberANDA090548
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateJune 7, 2017
Generic NameATORVASTATIN CALCIUM

INGREDIENTS (11)

ATORVASTATIN CALCIUM PROPYLENE GLYCOL SOLVATEActive
Quantity: 10 mg in 1 1
Code: YRZ789OWMI
Classification: ACTIM
CALCIUM ACETATEInactive
Code: Y882YXF34X
Classification: IACT
CROSCARMELLOSE SODIUMInactive
Code: M28OL1HH48
Classification: IACT
SODIUM CARBONATEInactive
Code: 45P3261C7T
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
HYPROMELLOSESInactive
Code: 3NXW29V3WO
Classification: IACT
HYDROXYPROPYL CELLULOSE (TYPE H)Inactive
Code: RFW2ET671P
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
POLYETHYLENE GLYCOL 8000Inactive
Code: Q662QK8M3B
Classification: IACT

ATORVASTATIN CALCIUM

PRODUCT DETAILS

NDC Product Code70882-109
Application NumberANDA090548
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateJune 7, 2017
Generic NameATORVASTATIN CALCIUM

INGREDIENTS (11)

CALCIUM ACETATEInactive
Code: Y882YXF34X
Classification: IACT
CROSCARMELLOSE SODIUMInactive
Code: M28OL1HH48
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
SODIUM CARBONATEInactive
Code: 45P3261C7T
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
HYDROXYPROPYL CELLULOSE (TYPE H)Inactive
Code: RFW2ET671P
Classification: IACT
HYPROMELLOSESInactive
Code: 3NXW29V3WO
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
POLYETHYLENE GLYCOL 8000Inactive
Code: Q662QK8M3B
Classification: IACT
ATORVASTATIN CALCIUM PROPYLENE GLYCOL SOLVATEActive
Quantity: 40 mg in 1 1
Code: YRZ789OWMI
Classification: ACTIM

ATORVASTATIN CALCIUM

PRODUCT DETAILS

NDC Product Code70882-120
Application NumberANDA090548
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateJune 7, 2017
Generic NameATORVASTATIN CALCIUM

INGREDIENTS (11)

CROSCARMELLOSE SODIUMInactive
Code: M28OL1HH48
Classification: IACT
CALCIUM ACETATEInactive
Code: Y882YXF34X
Classification: IACT
SODIUM CARBONATEInactive
Code: 45P3261C7T
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
POLYETHYLENE GLYCOL 8000Inactive
Code: Q662QK8M3B
Classification: IACT
HYPROMELLOSESInactive
Code: 3NXW29V3WO
Classification: IACT
HYDROXYPROPYL CELLULOSE (TYPE H)Inactive
Code: RFW2ET671P
Classification: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JP
Classification: IACT
ATORVASTATIN CALCIUM PROPYLENE GLYCOL SOLVATEActive
Quantity: 20 mg in 1 1
Code: YRZ789OWMI
Classification: ACTIM

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ATORVASTATIN CALCIUM - FDA Drug Approval Details