NDC 46708-681 – Albendazole

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

Human Prescription Drug

Product NDC46708-681

Product details

Brand name
Albendazole
Generic name
Albendazole
Labeler
Alembic Pharmaceuticals Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215652
Marketed since
September 11, 2024
Listing expires
December 31, 2026
Pharmacologic class
Anthelmintic

Active ingredients

Uses, dosage, side effects and warnings for Albendazole →

Package NDC codes (2)

Package NDCDescriptionSince
46708-681-022 TABLET, FILM COATED in 1 BOTTLE (46708-681-02)Sep 11, 2024
46708-681-2828 TABLET, FILM COATED in 1 BOTTLE (46708-681-28)Sep 11, 2024

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