Home > National Drug Code (NDC) > Mebendazole

Mebendazole - 0093-9107-29 - (Mebendazole)

Alphabetical Index


Drug Information of Mebendazole

Product NDC: 0093-9107
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: 0093-9107
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073580
Marketing Category: ANDA
Start Marketing Date: 20000623

Package Information of Mebendazole

Package NDC: 0093-9107-29
Package Description: 12 BLISTER PACK in 1 BOX (0093-9107-29) > 1 TABLET, CHEWABLE in 1 BLISTER PACK (0093-9107-19)

NDC Information of Mebendazole

NDC Code 0093-9107-29
Proprietary Name Mebendazole
Package Description 12 BLISTER PACK in 1 BOX (0093-9107-29) > 1 TABLET, CHEWABLE in 1 BLISTER PACK (0093-9107-19)
Product NDC 0093-9107
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Mebendazole
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20000623
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name MEBENDAZOLE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Antihelminthic [EPC]

Complete Information of Mebendazole


General Information