Ranitidine tablet

Ingredients and appearance - Product information

Ranitidine tablet- Ranitidine

Product information

Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC: 42708-118
Route of Administration Oral

Active Ingredient/Active Moiety

Ingredient Name Strength
Ranitidine hydrochloride ( UNII: BK76465IHM)( Ranitidine - UNII: 884KT10YB7 ) 150 mgin 1

Inactive Ingredients

Ingredient Name Code
Microcrystalline cellulose ( UNII: OP1R32D61U)
Croscarmellose ( UNII: 029TFK992N)
Fd&c yellow no. 6 ( UNII: H77VEI93A8)
Hypromellose, unspecified ( UNII: 3NXW29V3WO)
Magnesium stearate ( UNII: 70097M6I30)
Polydextrose ( UNII: VH2XOU12IE)
Silicon dioxide ( UNII: ETJ7Z6XBU4)
Titanium dioxide ( UNII: 15FIX9V2JP)
Triethyl citrate ( UNII: 8Z96QXD6UM)

Product Characteristics

Color ORANGE Size 9 mm
Shape ROUND Score 1
Imprint Code IP;253

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
ANDA ANDA077824 USA

Labeler - QPharma Inc( 030620888)

Establishment

Name ID/FEI Business Operations
QPharma Inc 030620888 REPACK( 42708-118)