Label: P- PACK PREDNISONE 20MG, 7- DAY TAPERING DOSE PACK- dr adam au tablet
- NDC Code(s): 85000-0011-1
- Packager: INTERSTELLAR PHARMACEUTICALS INC.
- This is a repackaged label.
- Source NDC Code(s): 0904-6923
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated November 29, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- PATIENT MEDICATION INFORMATION
- P-Pack Pednisone
-
INGREDIENTS AND APPEARANCE
P- PACK PREDNISONE 20MG, 7- DAY TAPERING DOSE PACK
dr adam au tabletProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:85000-0011(NDC:0904-6923) Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PREDNISONE (UNII: VB0R961HZT) (PREDNISONE - UNII:VB0R961HZT) PREDNISONE 10 mg Inactive Ingredients Ingredient Name Strength LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) Product Characteristics Color white Score 2 pieces Shape ROUND Size 9mm Flavor Imprint Code 5093;V Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:85000-0011-1 15 in 1 BOTTLE; Type 0: Not a Combination Product 07/12/2002 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA040256 07/12/2002 Labeler - INTERSTELLAR PHARMACEUTICALS INC. (130229096)
