ATORVASTATIN CALCIUM (Page 11 of 11)

Atorvastatin Calcium

Label ImageLabel Image
ATORVASTATIN CALCIUM atorvastatin calcium tablet, film coated
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68151-1013(NDC:60505-2579)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ATORVASTATIN CALCIUM PROPYLENE GLYCOL SOLVATE (ATORVASTATIN) ATORVASTATIN 20 mg
Inactive Ingredients
Ingredient Name Strength
CALCIUM ACETATE
CROSCARMELLOSE SODIUM
SODIUM CARBONATE
CELLULOSE, MICROCRYSTALLINE
MAGNESIUM STEARATE
SILICON DIOXIDE
HYPROMELLOSES
HYDROXYPROPYL CELLULOSE (TYPE H)
POLYETHYLENE GLYCOL 8000
TITANIUM DIOXIDE
Product Characteristics
Color WHITE Score no score
Shape OVAL Size 11mm
Flavor Imprint Code APO;ATV20
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:68151-1013-9 1 TABLET, FILM COATED in 1 PACKAGE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA090548 05/29/2012
Labeler — Carilion Materials Management (079239644)
Registrant — Carilion Materials Management (079239644)
Establishment
Name Address ID/FEI Operations
Carilion Materials Management 079239644 REPACK (68151-1013)

Revised: 06/2013 Carilion Materials Management

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