NDC 70518-0840 – Carvedilol

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

Human Prescription Drug

Product NDC70518-0840

Product details

Brand name
Carvedilol
Generic name
Carvedilol
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077614
Marketed since
November 10, 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 (1)

Package NDCDescriptionSince
70518-0840-250 POUCH in 1 BOX (70518-0840-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-0840-3)Apr 27, 2026

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