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Valium
Valium - 49349-765-01 - (diazepam)
Drug Information of Valium
| Product NDC: | 49349-765 |
| Proprietary Name: | Valium |
| Non Proprietary Name: | diazepam |
| Active Ingredient(s): | 5 mg/1 & nbsp; diazepam |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Valium
| Product NDC: | 49349-765 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA013263 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20121128 |
Package Information of Valium
| Package NDC: | 49349-765-01 |
| Package Description: | 1 TABLET in 1 BOTTLE (49349-765-01) |
NDC Information of Valium
| NDC Code | 49349-765-01 |
| Proprietary Name | Valium |
| Package Description | 1 TABLET in 1 BOTTLE (49349-765-01) |
| Product NDC | 49349-765 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | diazepam |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20121128 |
| Marketing Category Name | NDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | DIAZEPAM |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
