NDC 71335-0344 – Baclofen

Baclofen 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0344

Product details

Brand name
Baclofen
Generic name
Baclofen
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078220
Marketed since
July 1, 2007
Listing expires
December 31, 2026
Pharmacologic class
gamma-Aminobutyric Acid-ergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Baclofen →

Package NDC codes (10)

Package NDCDescriptionSince
71335-0344-0112 TABLET in 1 BOTTLE, PLASTIC (71335-0344-0)Feb 9, 2022
71335-0344-130 TABLET in 1 BOTTLE, PLASTIC (71335-0344-1)Feb 9, 2022
71335-0344-2120 TABLET in 1 BOTTLE, PLASTIC (71335-0344-2)Feb 9, 2022
71335-0344-320 TABLET in 1 BOTTLE, PLASTIC (71335-0344-3)Feb 9, 2022
71335-0344-460 TABLET in 1 BOTTLE, PLASTIC (71335-0344-4)Feb 9, 2022
71335-0344-5100 TABLET in 1 BOTTLE, PLASTIC (71335-0344-5)Feb 9, 2022
71335-0344-656 TABLET in 1 BOTTLE, PLASTIC (71335-0344-6)Feb 9, 2022
71335-0344-790 TABLET in 1 BOTTLE, PLASTIC (71335-0344-7)Feb 9, 2022
71335-0344-8140 TABLET in 1 BOTTLE, PLASTIC (71335-0344-8)Feb 9, 2022
71335-0344-984 TABLET in 1 BOTTLE, PLASTIC (71335-0344-9)Feb 9, 2022

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