Vigabatrin

NDC 42799-950 · Edenbridge Pharmaceuticals LLC.

Generic nameVigabatrin

Dosage formTABLET

RouteORAL

Active ingredient(s)VIGABATRIN

Strength500 mg/1

Pharmacologic classAnti-epileptic Agent [EPC]

Marketing categoryANDA

Packages

42799-950-01 — 100 TABLET in 1 BOTTLE (42799-950-01)

FDA lists these products with the same active ingredient.

0054-0652 — Vigabatrin, 0245-0556 — vigabatrin, 0245-6001 — Vigabatrin, 0591-3851 — Vigabatrin, 31722-009 — vigabatrin, 43598-651 — Vigabatrin, 43598-697 — Vigabatrin, 49884-358 — vigabatrin, 59651-366 — Vigabatrin, 59651-367 — Vigabatrin, 60219-1425 — Vigabatrin, 67386-111 — vigabatrin, 67386-211 — vigabatrin, 67877-674 — VIGABATRIN, 69097-964 — vigabatrin, 69238-1424 — Vigabatrin, 69238-1425 — Vigabatrin, 70710-1287 — vigabatrin, 70710-1494 — vigabatrin, 70771-1654 — vigabatrin, +4 more

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