NDC 70518-0356 – Carvedilol

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

Human Prescription Drug

Product NDC70518-0356

Product details

Brand name
Carvedilol
Generic name
Carvedilol
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077614
Marketed since
March 23, 2017
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
70518-0356-030 TABLET, FILM COATED in 1 BLISTER PACK (70518-0356-0)Mar 23, 2017
70518-0356-1180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0356-1)Oct 16, 2017

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