NDC 42291-093

Albendazole 200 mg

Albendazole

Albendazole 200 mg is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Avkare. The primary component is Albendazole.

Product ID42291-093_a5b0a8df-d830-55b3-e053-2995a90a1dbe
NDC42291-093
Product TypeHuman Prescription Drug
Proprietary NameAlbendazole 200 mg
Generic NameAlbendazole
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2020-05-15
Marketing CategoryANDA / ANDA
Application NumberANDA210011
Labeler NameAvKARE
Substance NameALBENDAZOLE
Active Ingredient Strength200 mg/1
Pharm ClassesAnthelmintic [EPC],Cytochrome P450 1A Inducers [MoA]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 42291-093-02

2 TABLET, FILM COATED in 1 BOTTLE (42291-093-02)
Marketing Start Date2020-05-15
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 42291-093-02 [42291009302]

Albendazole 200 mg TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA210011
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2020-05-15

Drug Details

NDC Crossover Matching brand name "Albendazole 200 mg" or generic name "Albendazole"

NDCBrand NameGeneric Name
0115-1701Albendazolealbendazole
0591-2712AlbendazoleAlbendazole
16714-907AlbendazoleAlbendazole
31722-935AlbendazoleAlbendazole
42291-093AlbendazoleAlbendazole
42799-110AlbendazoleAlbendazole
43598-452AlbendazoleAlbendazole
51407-258AlbendazoleAlbendazole
54505-055AlbendazoleAlbendazole
62980-513AlbendazoleAlbendazole
63629-1221AlbendazoleAlbendazole
63629-9278AlbendazoleAlbendazole
69097-237ALBENDAZOLEalbendazole
69539-151AlbendazoleAlbendazole
70710-1021AlbendazoleAlbendazole
52054-550ALBENZAalbendazole
55695-021ALBENZAalbendazole
64896-693ALBENZAalbendazole
65084-462ALBENZAalbendazole

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