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Baclofen

NDC 70710-1609 · Zydus Pharmaceuticals (USA) Inc.

Generic nameBaclofen
Dosage formTABLET
RouteORAL
Active ingredient(s)BACLOFEN
Strength5 mg/1
Pharmacologic classGABA A Agonists [MoA], GABA B Agonists [MoA], gamma-Aminobutyric Acid-ergic Agonist [EPC]
Marketing categoryANDA

Packages

70710-1609-1 — 100 TABLET in 1 BOTTLE (70710-1609-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-3614 — BACLOFEN, 70518-4235 — BACLOFEN, 70518-4249 — Baclofen, 70518-4290 — BACLOFEN, 70518-4378 — Baclofen, 70518-4384 — BACLOFEN, 70518-4530 — BACLOFEN, 70518-4656 — BACLOFEN, 70710-1285 — Baclofen, 70710-1286 — Baclofen, 70710-1666 — Baclofen, 70756-085 — Baclofen, 70756-288 — Baclofen, 70756-289 — Baclofen, 70771-1448 — Baclofen, 70771-1449 — Baclofen, 70771-1586 — Baclofen, 70771-1868 — Baclofen, 71205-474 — Baclofen, 71225-140 — 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.

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