BACLOFEN

NDC 59651-395 · Aurobindo Pharma Limited

Generic nameBACLOFEN

Dosage formTABLET

RouteORAL

Active ingredient(s)BACLOFEN

Strength20 mg/1

Pharmacologic classGABA A Agonists [MoA], GABA B Agonists [MoA], gamma-Aminobutyric Acid-ergic Agonist [EPC]

Marketing categoryANDA

Packages

59651-395-01 — 100 TABLET in 1 BOTTLE (59651-395-01)

59651-395-05 — 500 TABLET in 1 BOTTLE (59651-395-05)

59651-395-99 — 1000 TABLET in 1 BOTTLE (59651-395-99)

FDA lists these products with the same active ingredient.

55154-7635 — baclofen, 55154-7876 — baclofen, 55289-757 — Baclofen, 58657-730 — Baclofen, 58657-731 — Baclofen, 58657-732 — Baclofen, 58657-930 — Baclofen, 58657-931 — Baclofen, 58657-932 — Baclofen, 59651-394 — BACLOFEN, 60687-804 — Baclofen, 60687-815 — Baclofen, 60687-826 — Baclofen, 62135-472 — Baclofen, 62135-473 — Baclofen, 62135-474 — Baclofen, 62559-204 — Baclofen, 63187-147 — Baclofen, 63187-274 — Baclofen, 63187-280 — baclofen, +211 more

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