NDC 58657-751 – Carvedilol

Carvedilol 6.25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC58657-751

Product details

Brand name
Carvedilol
Generic name
Carvedilol
Labeler
Method Pharmaceuticals, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078786
Marketed since
December 3, 2024
Listing expires
December 31, 2026
Pharmacologic class
alpha-Adrenergic Blocker; beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Carvedilol →

Package NDC codes (2)

Package NDCDescriptionSince
58657-751-01100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (58657-751-01)Dec 3, 2024
58657-751-50500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (58657-751-50)Dec 3, 2024

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