NDC 43598-452 – Albendazole

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

Human Prescription Drug

Product NDC43598-452

Product details

Brand name
Albendazole
Generic name
Albendazole
Labeler
Dr.Reddys Laboratories Inc
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA211034
Marketed since
January 26, 2021
Listing expires
December 31, 2026
Pharmacologic class
Anthelmintic

Active ingredients

Uses, dosage, side effects and warnings for Albendazole →

Package NDC codes (3)

Package NDCDescriptionSince
43598-452-022 TABLET, FILM COATED in 1 BOTTLE (43598-452-02)Jan 26, 2021
43598-452-171 BLISTER PACK in 1 CARTON (43598-452-17) / 8 TABLET, FILM COATED in 1 BLISTER PACKJan 26, 2021
43598-452-6328 TABLET, FILM COATED in 1 BOTTLE (43598-452-63)Jan 26, 2021

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