VIGABATRIN

NDC 49884-358 · Par Health USA, LLC

Generic namevigabatrin

Dosage formPOWDER, FOR SOLUTION

RouteORAL

Active ingredient(s)VIGABATRIN

Strength50 mg/mL

Pharmacologic classAnti-epileptic Agent [EPC]

Marketing categoryANDA

Packages

49884-358-03 — 50 PACKET in 1 CARTON (49884-358-03) / 10 mL in 1 PACKET (49884-358-52)

FDA lists these products with the same active ingredient.

0054-0652 — Vigabatrin, 0245-0556 — vigabatrin, 0245-6001 — Vigabatrin, 0591-3851 — Vigabatrin, 31722-009 — vigabatrin, 42799-950 — Vigabatrin, 43598-651 — Vigabatrin, 43598-697 — 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 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.