NDC 68788-7539 – Carvedilol

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

Human Prescription Drug

Product NDC68788-7539

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 5, 2007
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
68788-7539-1100 TABLET, FILM COATED in 1 BOTTLE (68788-7539-1)Dec 27, 2019
68788-7539-330 TABLET, FILM COATED in 1 BOTTLE (68788-7539-3)Dec 27, 2019
68788-7539-660 TABLET, FILM COATED in 1 BOTTLE (68788-7539-6)Dec 27, 2019
68788-7539-990 TABLET, FILM COATED in 1 BOTTLE (68788-7539-9)Dec 27, 2019

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