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BACLOFEN

NDC 68788-8737 · 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

68788-8737-1 — 100 TABLET in 1 BOTTLE (68788-8737-1)

68788-8737-3 — 30 TABLET in 1 BOTTLE (68788-8737-3)

68788-8737-6 — 60 TABLET in 1 BOTTLE (68788-8737-6)

68788-8737-8 — 120 TABLET in 1 BOTTLE (68788-8737-8)

68788-8737-9 — 90 TABLET in 1 BOTTLE (68788-8737-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67296-2259 — BACLOFEN, 67544-671 — Baclofen, 68071-2289 — Baclofen, 68071-3407 — BACLOFEN, 68071-3700 — BACLOFEN, 68134-403 — Baclofen, 68788-4162 — Baclofen, 68788-8575 — BACLOFEN, 68788-8584 — BACLOFEN, 68788-8726 — BACLOFEN, 68788-8783 — Baclofen, 68788-9246 — baclofen, 69528-302 — Baclofen, 70121-2496 — baclofen, 70511-121 — Baclofen, 70511-122 — baclofen, 70511-123 — Baclofen, 70511-124 — Baclofen, 70512-782 — BACLOFEN, 70518-3089 — 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.