NDC 70518-1377 – Carvedilol

Carvedilol 3.125 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70518-1377

Product details

Brand name
Carvedilol
Generic name
Carvedilol
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077614
Marketed since
August 15, 2018
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 (4)

Package NDCDescriptionSince
70518-1377-030 TABLET, FILM COATED in 1 BLISTER PACK (70518-1377-0)Aug 15, 2018
70518-1377-1180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1377-1)Jul 9, 2019
70518-1377-5100 POUCH in 1 BOX (70518-1377-5) / 1 TABLET, FILM COATED in 1 POUCH (70518-1377-6)May 14, 2025
70518-1377-750 POUCH in 1 BOX (70518-1377-7) / 1 TABLET, FILM COATED in 1 POUCH (70518-1377-6)Apr 24, 2026

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