Tiagabine Hydrochloride 62756-0200

Product NDC

62756-0200

Manufacturer: Sun Pharmaceutical Industries, Inc.
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: November 4, 2011
Listing Expires: December 31, 2026
Application: ANDA077555

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Active Ingredients

Ingredient	Strength
Tiagabine Hydrochloride	2 mg/1

Drug Class

Anti-epileptic Agent [EPC]Decreased Central Nervous System Disorganized Electrical Activity [PE]

Packaging Options(2)

62756-0200-18

1000 TABLET, FILM COATED in 1 BOTTLE (62756-200-18)

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62756-0200-83

30 TABLET, FILM COATED in 1 BOTTLE (62756-200-83)

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