NDC 62756-0200-83

TIAGABINE HYDROCHLORIDE 2 mg/1 TABLET, FILM COATED

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NDC

62756-0200-83

Generic Name

TIAGABINE HYDROCHLORIDE

Brand Name

TIAGABINE HYDROCHLORIDE

Strength

2 mg/1

Dosage Form

TABLET, FILM COATED

Route

ORAL

Package Size

—

Labeler

Sun Pharmaceutical Industries, Inc.

FDA Drug Information

Indications & Usage

INDICATIONS AND USAGE Tiagabine hydrochloride tablets are indicated as adjunctive therapy in adults and children 12 years and older in the treatment of partial seizures.

Important Warnings

WARNINGS Seizures in Patients Without Epilepsy: Postmarketing reports have shown that tiagabine hydrochloride use has been associated with new onset seizures and status epilepticus in patients without epilepsy. Dose may be an important predisposing factor in the development of seizures, although seizures have been reported in patients taking daily doses of tiagabine hydrochloride as low as 4 mg/da…

Source: FDA. For professional use only. Not a substitute for prescribing information.

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Other TIAGABINE HYDROCHLORIDE NDC Codes

62756-0224-834 mg/1TABLET, FILM COATED

2-Day

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