Prednisone tablet

Ingredients and appearance - Product information

Prednisone tablet- Prednisone

Product information

Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC: 42708-115
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, unspecified ( UNII: 2S7830E561)
Docusate sodium ( UNII: F05Q2T2JA0)
Magnesium stearate ( UNII: 70097M6I30)
Sodium benzoate ( UNII: OJ245FE5EU)

Product Characteristics

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

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
ANDA ANDA085162 USA

Labeler - QPharma Inc( 030620888)

Establishment

Name ID/FEI Business Operations
QPharma Inc 030620888 REPACK( 42708-115)