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Mebendazole
Mebendazole - 0093-9107-29 - (Mebendazole)
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] |
