NDC 63629-1221

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 Bryant Ranch Prepack. The primary component is Albendazole.

Product ID63629-1221_4f7be12b-5c5f-4075-b4e5-c45d6ea6233a
NDC63629-1221
Product TypeHuman Prescription Drug
Proprietary NameAlbendazole 200 mg
Generic NameAlbendazole
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2018-12-15
Marketing CategoryANDA / ANDA
Application NumberANDA210011
Labeler NameBryant Ranch Prepack
Substance NameALBENDAZOLE
Active Ingredient Strength200 mg/1
Pharm ClassesAnthelmintic [EPC],Cytochrome P450 1A Inducers [MoA]
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 63629-1221-1

2 TABLET, FILM COATED in 1 BOTTLE (63629-1221-1)
Marketing Start Date2021-01-14
NDC Exclude FlagN
Sample Package?N

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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