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DARANIDE
DARANIDE - 51672-4144-1 - (dichlorphenamide)
Drug Information of DARANIDE
| Product NDC: | 51672-4144 |
| Proprietary Name: | DARANIDE |
| Non Proprietary Name: | dichlorphenamide |
| Active Ingredient(s): | 50 mg/1 & nbsp; dichlorphenamide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DARANIDE
| Product NDC: | 51672-4144 |
| Labeler Name: | Taro Pharmaceuticals U.S.A., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA011366 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120316 |
Package Information of DARANIDE
| Package NDC: | 51672-4144-1 |
| Package Description: | 100 TABLET in 1 BOTTLE (51672-4144-1) |
NDC Information of DARANIDE
| NDC Code | 51672-4144-1 |
| Proprietary Name | DARANIDE |
| Package Description | 100 TABLET in 1 BOTTLE (51672-4144-1) |
| Product NDC | 51672-4144 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | dichlorphenamide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120316 |
| Marketing Category Name | NDA |
| Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
| Substance Name | DICHLORPHENAMIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
