Prednisone tablet

Ingredients and appearance - Product information

Prednisone tablet- Prednisone

Product information

Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC: 42708-046
Route of Administration Oral

Active Ingredient/Active Moiety

Ingredient Name Strength
Prednisone ( UNII: VB0R961HZT)( Prednisone - UNII: VB0R961HZT ) 20 mgin 1

Inactive Ingredients

Ingredient Name Code
Fd&c yellow no. 6 ( UNII: H77VEI93A8)
Lactose monohydrate ( UNII: EWQ57Q8I5X)
Magnesium stearate ( UNII: 70097M6I30)
Microcrystalline cellulose ( UNII: OP1R32D61U)
Sodium starch glycolate type a potato ( UNII: 5856J3G2A2)

Product Characteristics

Color ORANGE (peach) Size 10 mm
Shape ROUND Score 2
Imprint Code 5092;V

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
ANDA ANDA040392 USA

Labeler - QPharma Inc( 030620888)

Establishment

Name ID/FEI Business Operations
QPharma Inc 030620888 REPACK( 42708-046)