Amlodipine Besylate and Benazepril Hydrochloride (Page 7 of 7)

Amlodipine Besylate/Benazepril 5/10mg

Label ImageLabel Image
AMLODIPINE BESYLATE AND BENAZEPRIL HYDROCHLORIDE amlodipine besylate and benazepril hydrochloride capsule
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68151-1364(NDC:68180-756)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
AMLODIPINE BESYLATE (AMLODIPINE) AMLODIPINE 5 mg
BENAZEPRIL HYDROCHLORIDE (BENAZEPRILAT) BENAZEPRIL HYDROCHLORIDE 10 mg
Inactive Ingredients
Ingredient Name Strength
ANHYDROUS LACTOSE
FERRIC OXIDE YELLOW
GELATIN, UNSPECIFIED
SILICON DIOXIDE
MICROCRYSTALLINE CELLULOSE
CROSPOVIDONE (15 MPA.S AT 5%)
SHELLAC
POVIDONE, UNSPECIFIED
POTASSIUM HYDROXIDE
MAGNESIUM STEARATE
PROPYLENE GLYCOL
TITANIUM DIOXIDE
FERROSOFERRIC OXIDE
FERRIC OXIDE RED
Product Characteristics
Color BROWN (Light Brown Opaque Cap and Light Brown Opaque Body) Score no score
Shape CAPSULE Size 18mm
Flavor Imprint Code LU;E12
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:68151-1364-0 1 CAPSULE in 1 PACKAGE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA078466 02/05/2010
Labeler — Carilion Materials Management (079239644)
Establishment
Name Address ID/FEI Operations
Carilion Materials Management 079239644 REPACK (68151-1364)

Revised: 07/2017 Carilion Materials Management

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