SUMATRIPTAN- sumatriptan succinate tablet

Sumatriptan by

Drug Labeling and Warnings

Sumatriptan by is a Prescription medication manufactured, distributed, or labeled by Bryant Ranch Prepack. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Sumatriptan Succinate Tablets

HOW SUPPLIED

Product: 63629-8134

NDC: 63629-8134-1 9 TABLET in a BOTTLE

Product: 63629-8188

NDC: 63629-8188-1 9 TABLET in a BOTTLE

SUMATRIPTAN 50MG TABLET

SUMATRIPTAN SUCCINATE 100MG TAB

INGREDIENTS AND APPEARANCE

SUMATRIPTAN 
sumatriptan succinate tablet

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 63629-8134(NDC:65862-147)
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SUMATRIPTAN SUCCINATE (UNII: J8BDZ68989) (SUMATRIPTAN - UNII:8R78F6L9VO)	SUMATRIPTAN	50 mg

Inactive Ingredients
Ingredient Name	Strength
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)

Product Characteristics
Color	WHITE (White to off-white)	Score	no score
Shape	CAPSULE (biconvex)	Size	11mm
Flavor		Imprint Code	C;33
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63629-8134-1	9 in 1 BOTTLE; Type 0: Not a Combination Product	07/29/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA078327	08/17/2009

SUMATRIPTAN 
sumatriptan succinate tablet

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 63629-8188(NDC:65862-148)
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SUMATRIPTAN SUCCINATE (UNII: J8BDZ68989) (SUMATRIPTAN - UNII:8R78F6L9VO)	SUMATRIPTAN	100 mg

Inactive Ingredients
Ingredient Name	Strength
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)

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	Marketing Start Date	Marketing End Date
1	NDC: 63629-8188-1	9 in 1 BOTTLE; Type 0: Not a Combination Product	08/02/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA078327	08/17/2009

Labeler - Bryant Ranch Prepack (171714327)

Establishment
Name	Address	ID/FEI	Business Operations
Bryant Ranch Prepack		171714327	REPACK(63629-8188, 63629-8134) , RELABEL(63629-8134, 63629-8188)