Prednisone tablet

Ingredients and appearance - Product information

Prednisone tablet- Prednisone

Product information

Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC: 67296-0140
Route of Administration Oral

Active Ingredient/Active Moiety

Ingredient Name Strength
Prednisone ( UNII: VB0R961HZT)( Prednisone - UNII: VB0R961HZT ) 10 mgin 1

Inactive Ingredients

Ingredient Name Code
Anhydrous lactose ( UNII: 3SY5LH9PMK)
Silicon dioxide ( UNII: ETJ7Z6XBU4)
Crospovidone ( UNII: 68401960MK)
Docusate sodium ( UNII: F05Q2T2JA0)
Magnesium stearate ( UNII: 70097M6I30)
Sodium benzoate ( UNII: OJ245FE5EU)

Product Characteristics

Color white Score 2
Shape ROUND Imprint Code DAN;DAN;5442
Size 9 mm

Packaging

# Item Code Package Description Marketing Start Date
1 NDC: 67296-0140-2 30 in 1 BOTTLE 2011/06/24
2 NDC: 67296-0140-1 10 in 1 BOTTLE 2020/04/22
3 NDC: 67296-0140-9 9 in 1 BOTTLE 2020/04/22
4 NDC: 67296-0140-3 42 in 1 BOTTLE 2020/04/22

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
ANDA ANDA085162 USA 2020/04/22

Labeler - RedPharm Drug Inc.( 828374897)

Establishment

Name ID/FEI Business Operations
RedPharm Drug Inc. 828374897 label( 67296-0140), repack( 67296-0140)