NDC Code(s) : 63629-4017-1, 63629-4017-2, 63629-4017-3, 63629-4017-4, 63629-4017-5, 63629-4017-6, 63629-4017-7, 63629-4017-8
Packager : Bryant Ranch Prepack

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Warfarin SodiumWarfarin Sodium TABLET
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:63629-4017(NDC:68382-052)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
WARFARIN SODIUM(UNII: 6153CWM0CL)
(WARFARIN - UNII:5Q7ZVV76EI) 		WARFARIN SODIUM1 mg
Inactive Ingredients
Ingredient Name Strength
D&C RED NO. 6(UNII: 481744AI4O)
HYDROXYPROPYL CELLULOSE (1200000 MW)(UNII: RFW2ET671P)
LACTOSE MONOHYDRATE(UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE(UNII: 70097M6I30)
STARCH, CORN(UNII: O8232NY3SJ)
Product Characteristics
Color PINK (PINK) Score 2 pieces
Shape OVAL (OVAL) Size 11 mm
Flavor Imprint Code WAR;1
Contains
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:63629-4017-1 30 in 1 BOTTLE Type 0: Not a Combination Product19/06/2006
2NDC:63629-4017-2 60 in 1 BOTTLE Type 0: Not a Combination Product19/06/2006
3NDC:63629-4017-3 100 in 1 BOTTLE Type 0: Not a Combination Product19/06/2006
4NDC:63629-4017-4 50 in 1 BOTTLE Type 0: Not a Combination Product10/06/2009
5NDC:63629-4017-5 90 in 1 BOTTLE Type 0: Not a Combination Product10/06/2009
6NDC:63629-4017-6 21 in 1 BOTTLE Type 0: Not a Combination Product10/06/2009
7NDC:63629-4017-7 15 in 1 BOTTLE Type 0: Not a Combination Product10/06/2009
8NDC:63629-4017-8 20 in 1 BOTTLE Type 0: Not a Combination Product10/06/2009
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA040663 06/19/2006

PRINCIPAL DISPLAY PANEL

Label Image