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Amlodipine Besylate and Benazepril Hydrochloride

These highlights do not include all the information needed to use amlodipine besylate and benazepril hydrochloride capsules safely and effectively. See full prescribing information for amlodipine besylate and benazepril hydrochloride capsules.   Amlodipine Besylate and Benazepril Hydrochloride Capsules Initial U.S. Approval: 1995

Approved
Approval ID

15f7cde7-8dc2-4b07-83a9-9b86d6ec7f43

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Dec 20, 2011

Manufacturers
FDA

Rebel Distributors Corp

DUNS: 118802834

Products 2

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

Amlodipine Besylate and Benazepril Hydrochloride

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code42254-074
Application NumberANDA090149
Product Classification
M
Marketing Category
C73584
G
Generic Name
Amlodipine Besylate and Benazepril Hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateJanuary 10, 2011
FDA Product Classification

INGREDIENTS (14)

amlodipine besylateActive
Quantity: 10 mg in 1 1
Code: 864V2Q084H
Classification: ACTIM
crospovidoneInactive
Code: 68401960MK
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
lactose monohydrateInactive
Code: EWQ57Q8I5X
Classification: IACT
magnesium stearateInactive
Code: 70097M6I30
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
talcInactive
Code: 7SEV7J4R1U
Classification: IACT
D&C YELLOW NO. 10Inactive
Code: 35SW5USQ3G
Classification: IACT
D&C RED NO. 28Inactive
Code: 767IP0Y5NH
Classification: IACT
gelatinInactive
Code: 2G86QN327L
Classification: IACT
titanium dioxideInactive
Code: 15FIX9V2JP
Classification: IACT
benazepril hydrochlorideActive
Quantity: 40 mg in 1 1
Code: N1SN99T69T
Classification: ACTIB
SODIUM STARCH GLYCOLATE TYPE A POTATOInactive
Code: 5856J3G2A2
Classification: IACT
sodium lauryl sulfateInactive
Code: 368GB5141J
Classification: IACT

Amlodipine Besylate and Benazepril Hydrochloride

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code42254-073
Application NumberANDA090149
Product Classification
M
Marketing Category
C73584
G
Generic Name
Amlodipine Besylate and Benazepril Hydrochloride
Product Specifications
Route of AdministrationORAL
Effective DateJanuary 10, 2011
FDA Product Classification

INGREDIENTS (15)

benazepril hydrochlorideActive
Quantity: 40 mg in 1 1
Code: N1SN99T69T
Classification: ACTIB
amlodipine besylateActive
Quantity: 5 mg in 1 1
Code: 864V2Q084H
Classification: ACTIM
crospovidoneInactive
Code: 68401960MK
Classification: IACT
lactose monohydrateInactive
Code: EWQ57Q8I5X
Classification: IACT
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
magnesium stearateInactive
Code: 70097M6I30
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
SODIUM STARCH GLYCOLATE TYPE A POTATOInactive
Code: 5856J3G2A2
Classification: IACT
talcInactive
Code: 7SEV7J4R1U
Classification: IACT
FD&C RED NO. 40Inactive
Code: WZB9127XOA
Classification: IACT
FD&C BLUE NO. 1Inactive
Code: H3R47K3TBD
Classification: IACT
gelatinInactive
Code: 2G86QN327L
Classification: IACT
titanium dioxideInactive
Code: 15FIX9V2JP
Classification: IACT
FD&C YELLOW NO. 6Inactive
Code: H77VEI93A8
Classification: IACT
sodium lauryl sulfateInactive
Code: 368GB5141J
Classification: IACT

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Amlodipine Besylate and Benazepril Hydrochloride - FDA Drug Approval Details