NDC 68788-8252 – Carvedilol

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

Human Prescription Drug

Product NDC68788-8252

Product details

Brand name
Carvedilol
Generic name
Carvedilol
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077614
Marketed since
September 2, 2022
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 (5)

Package NDCDescriptionSince
68788-8252-1100 TABLET, FILM COATED in 1 BOTTLE (68788-8252-1)Sep 2, 2022
68788-8252-330 TABLET, FILM COATED in 1 BOTTLE (68788-8252-3)Sep 2, 2022
68788-8252-660 TABLET, FILM COATED in 1 BOTTLE (68788-8252-6)Sep 2, 2022
68788-8252-8120 TABLET, FILM COATED in 1 BOTTLE (68788-8252-8)Sep 2, 2022
68788-8252-990 TABLET, FILM COATED in 1 BOTTLE (68788-8252-9)Sep 2, 2022

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