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BACLOFEN

NDC 72789-312 · PD-Rx 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

72789-312-30 — 30 TABLET in 1 BOTTLE, PLASTIC (72789-312-30)

72789-312-90 — 90 TABLET in 1 BOTTLE, PLASTIC (72789-312-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72162-1080 — baclofen, 72162-1152 — Baclofen, 72162-2372 — Baclofen, 72162-2373 — Baclofen, 72162-2374 — Baclofen, 72162-2448 — Baclofen, 72162-2449 — Baclofen, 72162-2450 — Baclofen, 72189-504 — Baclofen, 72189-565 — Baclofen, 72789-478 — BACLOFEN, 72789-479 — BACLOFEN, 72789-480 — BACLOFEN, 72789-508 — BACLOFEN, 72834-602 — Baclofen, 72865-296 — BACLOFEN, 72865-297 — BACLOFEN, 72865-298 — BACLOFEN, 72888-009 — BACLOFEN, 72888-010 — BACLOFEN, +211 more

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels