NDC 0591-2712 – Albendazole

Albendazole 200 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC0591-2712

Product details

Brand name
Albendazole
Generic name
Albendazole
Labeler
Actavis Pharma, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208094
Marketed since
June 13, 2019
Listing expires
December 31, 2026
Pharmacologic class
Anthelmintic

Active ingredients

Uses, dosage, side effects and warnings for Albendazole →

Package NDC codes (1)

Package NDCDescriptionSince
0591-2712-022 TABLET, FILM COATED in 1 BOTTLE (0591-2712-02)Jun 13, 2019

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