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MEBENDAZOLE
MEBENDAZOLE - 54868-3732-2 - (mebendazole)
Drug Information of MEBENDAZOLE
| Product NDC: | 54868-3732 |
| 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: | 54868-3732 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA073580 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19960404 |
Package Information of MEBENDAZOLE
| Package NDC: | 54868-3732-2 |
| Package Description: | 1 BLISTER PACK in 1 BOTTLE, DISPENSING (54868-3732-2) > 6 TABLET, CHEWABLE in 1 BLISTER PACK |
NDC Information of MEBENDAZOLE
| NDC Code | 54868-3732-2 |
| Proprietary Name | MEBENDAZOLE |
| Package Description | 1 BLISTER PACK in 1 BOTTLE, DISPENSING (54868-3732-2) > 6 TABLET, CHEWABLE in 1 BLISTER PACK |
| Product NDC | 54868-3732 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | mebendazole |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 19960404 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | MEBENDAZOLE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antihelminthic [EPC] |
