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BACLOFEN

NDC 71335-0949 · Bryant Ranch Prepack

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

71335-0949-0 120 TABLET in 1 BOTTLE (71335-0949-0)

71335-0949-1 90 TABLET in 1 BOTTLE (71335-0949-1)

71335-0949-2 20 TABLET in 1 BOTTLE (71335-0949-2)

71335-0949-3 60 TABLET in 1 BOTTLE (71335-0949-3)

71335-0949-4 45 TABLET in 1 BOTTLE (71335-0949-4)

71335-0949-5 112 TABLET in 1 BOTTLE (71335-0949-5)

71335-0949-6 30 TABLET in 1 BOTTLE (71335-0949-6)

71335-0949-7 56 TABLET in 1 BOTTLE (71335-0949-7)

71335-0949-8 15 TABLET in 1 BOTTLE (71335-0949-8)

71335-0949-9 84 TABLET in 1 BOTTLE (71335-0949-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70756-288 — Baclofen, 70756-289 — Baclofen, 70771-1448 — Baclofen, 70771-1449 — Baclofen, 70771-1586 — Baclofen, 70771-1868 — Baclofen, 71205-474 — Baclofen, 71225-140 — BACLOFEN, 71335-0103 — baclofen, 71335-0344 — baclofen, 71335-1356 — Baclofen, 71335-1796 — Baclofen, 71335-1797 — Baclofen, 71335-2219 — BACLOFEN, 71335-2392 — Baclofen, 71335-2482 — Baclofen, 71335-2497 — BACLOFEN, 71335-2668 — Baclofen, 71335-2669 — Baclofen, 71335-2756 — 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.