Allopurinol tablet

Ingredients and appearance - Product information

Allopurinol tablet- Allopurinol

Product information

Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC: 49349-119
Route of Administration Oral

Active Ingredient/Active Moiety

Ingredient Name Strength
Allopurinol ( UNII: 63CZ7GJN5I)( Allopurinol - UNII: 63CZ7GJN5I ) 100 mgin 1

Inactive Ingredients

Ingredient Name Code
Croscarmellose sodium ( UNII: M28OL1HH48)
Lactose monohydrate ( UNII: EWQ57Q8I5X)
Magnesium stearate ( UNII: 70097M6I30)
Cellulose, microcrystalline ( UNII: OP1R32D61U)
Starch, corn ( UNII: O8232NY3SJ)
Sodium lauryl sulfate ( UNII: 368GB5141J)

Product Characteristics

Color white Imprint Code DAN;DAN;5543
Score 2 Shape ROUND
Size 10 mm

Packaging

# Item Code Package Description Marketing Start Date
1 NDC: 49349-119-02 30 in 1 BLISTER PACK 2009/09/03
2 NDC: 49349-119-19 90 in 1 BOTTLE, PLASTIC 2017/09/19

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
NDA NDA018832 USA 2017/09/19

Labeler - REMEDYREPACK INC.( 829572556)