BACLOFEN

NDC 68788-8575 · Preferred Pharmaceuticals Inc.

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

68788-8575-3 — 30 TABLET in 1 BOTTLE (68788-8575-3)

68788-8575-9 — 90 TABLET in 1 BOTTLE (68788-8575-9)

FDA lists these products with the same active ingredient.

66794-157 — Baclofen Injection, 67046-1072 — Baclofen, 67296-1947 — Baclofen, 67296-2259 — BACLOFEN, 67544-671 — Baclofen, 68071-2289 — Baclofen, 68071-3407 — BACLOFEN, 68071-3700 — BACLOFEN, 68134-403 — Baclofen, 68788-4162 — Baclofen, 68788-8584 — BACLOFEN, 68788-8726 — BACLOFEN, 68788-8737 — BACLOFEN, 68788-8783 — Baclofen, 68788-9246 — baclofen, 69528-302 — Baclofen, 70121-2496 — baclofen, 70511-121 — Baclofen, 70511-122 — baclofen, 70511-123 — Baclofen, +211 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.