NDC 70518-2389 – Carvedilol

Carvedilol 25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70518-2389

Product details

Brand name
Carvedilol
Generic name
Carvedilol
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077614
Marketed since
October 25, 2019
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
70518-2389-130 TABLET, FILM COATED in 1 BLISTER PACK (70518-2389-1)Jan 22, 2026
70518-2389-2180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2389-2)Jul 30, 2026

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