NDC 0115-1701 – Albendazole

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

Human Prescription Drug

Product NDC0115-1701

Product details

Brand name
Albendazole
Generic name
Albendazole
Labeler
Amneal Pharmaceuticals of New York LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA020666
Marketed since
June 11, 1996
Listing expires
December 31, 2026
Pharmacologic class
Anthelmintic

Active ingredients

Uses, dosage, side effects and warnings for Albendazole →

Package NDC codes (1)

Package NDCDescriptionSince
0115-1701-492 TABLET, FILM COATED in 1 BOTTLE (0115-1701-49)Jun 11, 1996

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