NDC 42806-039 – Betaxolol

Betaxolol Hydrochloride 20 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC42806-039

Product details

Brand name
Betaxolol
Generic name
Betaxolol
Labeler
Epic Pharma LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA075541
Marketed since
July 20, 2010
Listing expires
December 31, 2026
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Betaxolol →

Package NDC codes (2)

Package NDCDescriptionSince
42806-039-01100 TABLET, FILM COATED in 1 BOTTLE (42806-039-01)Jul 20, 2010
42806-039-101000 TABLET, FILM COATED in 1 BOTTLE (42806-039-10)Jul 20, 2010

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