Topiramate

NDC 47335-707 · Sun Pharmaceutical Industries, Inc.

Generic nameTopiramate

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)TOPIRAMATE

Strength25 mg/1

Pharmacologic classCytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 3A4 Inducers [MoA], Decreased Central Nervous System Disorganized Electrical Activity [PE]

Marketing categoryANDA

Packages

47335-707-08 — 100 TABLET, FILM COATED in 1 BOTTLE (47335-707-08)

47335-707-18 — 1000 TABLET, FILM COATED in 1 BOTTLE (47335-707-18)

47335-707-83 — 30 TABLET, FILM COATED in 1 BOTTLE (47335-707-83)

47335-707-86 — 60 TABLET, FILM COATED in 1 BOTTLE (47335-707-86)

47335-707-88 — 100 TABLET, FILM COATED in 1 BOTTLE (47335-707-88)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

43063-997 — Topiramate, 43063-998 — Topiramate, 43598-624 — Phentermine and Topiramate Extended-Release, 43598-625 — Phentermine and Topiramate Extended-Release, 43598-626 — Phentermine and Topiramate Extended-Release, 43598-627 — Phentermine and Topiramate Extended-Release, 43598-939 — Topiramate, 43598-940 — Topiramate, 43598-941 — Topiramate, 43598-942 — Topiramate, 47335-710 — Topiramate, 47335-711 — Topiramate, 47335-712 — Topiramate, 50090-2102 — topiramate, 50090-2203 — topiramate, 50090-3389 — Topiramate, 50090-3461 — Topiramate, 50090-4614 — Topiramate, 50090-5309 — topiramate, 50090-5853 — topiramate, +289 more

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