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Mebendazole - 63629-1528-1 - (Mebendazole)

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Drug Information of Mebendazole

Product NDC: 63629-1528
Proprietary Name: Mebendazole
Non Proprietary Name: Mebendazole
Active Ingredient(s): 100    mg/1 & nbsp;   Mebendazole
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of Mebendazole

Product NDC: 63629-1528
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073580
Marketing Category: ANDA
Start Marketing Date: 20100428

Package Information of Mebendazole

Package NDC: 63629-1528-1
Package Description: 2 TABLET, CHEWABLE in 1 BOTTLE (63629-1528-1)

NDC Information of Mebendazole

NDC Code 63629-1528-1
Proprietary Name Mebendazole
Package Description 2 TABLET, CHEWABLE in 1 BOTTLE (63629-1528-1)
Product NDC 63629-1528
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mebendazole
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20100428
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name MEBENDAZOLE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Antihelminthic [EPC]

Complete Information of Mebendazole


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