Oxaprozin (Page 7 of 7)

Pramipexole Dihydrochloride 0.125 tabs

Label ImageLabel Image
OXAPROZIN
oxaprozin tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68151-0523(NDC:0185-0141)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
OXAPROZIN (OXAPROZIN) OXAPROZIN 600 mg
Inactive Ingredients
Ingredient Name Strength
SILICON DIOXIDE
HYPROMELLOSE, UNSPECIFIED
MAGNESIUM STEARATE
METHYLCELLULOSE (100 MPA.S)
MICROCRYSTALLINE CELLULOSE
POLACRILIN POTASSIUM
POLYETHYLENE GLYCOL, UNSPECIFIED
POLYSORBATE 80
STARCH, CORN
TITANIUM DIOXIDE
Product Characteristics
Color WHITE Score 2 pieces
Shape CAPSULE Size 19mm
Flavor Imprint Code E;141
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:68151-0523-0 1 TABLET in 1 PACKAGE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA075845 01/31/2001
Labeler — Carilion Materials Management (079239644)
Establishment
Name Address ID/FEI Operations
Carilion Materials Management 079239644 REPACK (68151-0523)

Revised: 07/2017 Carilion Materials Management

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