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Tiagabine Hydrochloride

NDC 72205-085 · Novadoz Pharmaceuticals LLC

Generic nameTiagabine Hydrochloride
Dosage formTABLET
RouteORAL
Active ingredient(s)TIAGABINE HYDROCHLORIDE
Strength4 mg/1
Pharmacologic classAnti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE]
Marketing categoryANDA

Packages

72205-085-30 — 30 TABLET in 1 BOTTLE (72205-085-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0093-5030 — Tiagabine Hydrochloride, 0093-5031 — Tiagabine Hydrochloride, 0093-8072 — Tiagabine Hydrochloride, 0093-8076 — Tiagabine Hydrochloride, 62756-200 — TIAGABINE HYDROCHLORIDE, 62756-224 — TIAGABINE HYDROCHLORIDE, 72205-084 — Tiagabine Hydrochloride, 72205-086 — Tiagabine Hydrochloride, 72205-087 — Tiagabine Hydrochloride

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.