NDC 58657-732 – Baclofen

Baclofen 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC58657-732

Product details

Brand name
Baclofen
Generic name
Baclofen
Labeler
Method Pharmaceuticals LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA212378
Marketed since
June 15, 2024
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 (3)

Package NDCDescriptionSince
58657-732-01100 TABLET in 1 BOTTLE (58657-732-01)Jun 15, 2024
58657-732-101000 TABLET in 1 BOTTLE (58657-732-10)Jun 15, 2024
58657-732-50500 TABLET in 1 BOTTLE (58657-732-50)Jun 15, 2024

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