NDC 71335-9681 – Baclofen

Baclofen 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-9681

Product details

Brand name
Baclofen
Generic name
Baclofen
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077068
Marketed since
August 30, 2005
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
71335-9681-0120 TABLET in 1 BOTTLE, PLASTIC (71335-9681-0)Dec 12, 2024
71335-9681-190 TABLET in 1 BOTTLE, PLASTIC (71335-9681-1)Dec 12, 2024
71335-9681-220 TABLET in 1 BOTTLE, PLASTIC (71335-9681-2)Dec 12, 2024
71335-9681-360 TABLET in 1 BOTTLE, PLASTIC (71335-9681-3)Dec 12, 2024
71335-9681-445 TABLET in 1 BOTTLE, PLASTIC (71335-9681-4)Dec 12, 2024
71335-9681-5112 TABLET in 1 BOTTLE, PLASTIC (71335-9681-5)Dec 12, 2024
71335-9681-630 TABLET in 1 BOTTLE, PLASTIC (71335-9681-6)Dec 12, 2024
71335-9681-756 TABLET in 1 BOTTLE, PLASTIC (71335-9681-7)Dec 12, 2024
71335-9681-815 TABLET in 1 BOTTLE, PLASTIC (71335-9681-8)Dec 12, 2024
71335-9681-984 TABLET in 1 BOTTLE, PLASTIC (71335-9681-9)Dec 12, 2024

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