NDC 68788-9789 – Carvedilol

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

Human Prescription Drug

Product NDC68788-9789

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
June 4, 2012
Listing expires
December 31, 2026
Pharmacologic class
alpha-Adrenergic Blocker; beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Carvedilol →

Package NDC codes (4)

Package NDCDescriptionSince
68788-9789-1100 TABLET, FILM COATED in 1 BOTTLE (68788-9789-1)Jun 4, 2012
68788-9789-330 TABLET, FILM COATED in 1 BOTTLE (68788-9789-3)Jun 4, 2012
68788-9789-660 TABLET, FILM COATED in 1 BOTTLE (68788-9789-6)Jun 4, 2012
68788-9789-990 TABLET, FILM COATED in 1 BOTTLE (68788-9789-9)Jun 4, 2012

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