Prescription Drug Information: Sumatriptan

SUMATRIPTAN- sumatriptan succinate tablet
NuCare Pharmaceuticals,Inc.

Sumatriptan Succinate Tablets

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL —

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SUMATRIPTAN
sumatriptan succinate tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:68071-5072(NDC:65862-148)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
SUMATRIPTAN SUCCINATE (SUMATRIPTAN) SUMATRIPTAN 100 mg
Inactive Ingredients
Ingredient Name Strength
CROSCARMELLOSE SODIUM
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS
MAGNESIUM STEARATE
MICROCRYSTALLINE CELLULOSE
POLYSORBATE 80
SODIUM BICARBONATE
Product Characteristics
Color white (White to off-white) Score no score
Shape CAPSULE (biconvex) Size 12mm
Flavor Imprint Code C;34
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:68071-5072-9 9 TABLET in 1 BOX None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA078327 08/17/2009
Labeler — NuCare Pharmaceuticals,Inc. (010632300)
Establishment
Name Address ID/FEI Operations
NuCare Pharmaceuticals,Inc. 010632300 relabel (68071-5072)

Revised: 02/2021 NuCare Pharmaceuticals,Inc.

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