NDC 70518-4389 – Carvedilol

Carvedilol 12.5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70518-4389

Product details

Brand name
Carvedilol
Generic name
Carvedilol
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077614
Marketed since
July 8, 2025
Listing expires
December 31, 2027
Pharmacologic class
alpha-Adrenergic Blocker; beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Carvedilol →

Package NDC codes (2)

Package NDCDescriptionSince
70518-4389-030 TABLET, FILM COATED in 1 BLISTER PACK (70518-4389-0)Jul 8, 2025
70518-4389-130 TABLET, FILM COATED in 1 BLISTER PACK (70518-4389-1)Aug 19, 2025

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