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DIAZEPAM
DIAZEPAM - 16590-071-75 - (DIAZEPAM)
Drug Information of DIAZEPAM
| Product NDC: | 16590-071 |
| Proprietary Name: | DIAZEPAM |
| Non Proprietary Name: | DIAZEPAM |
| Active Ingredient(s): | 10 mg/1 & nbsp; DIAZEPAM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DIAZEPAM
| Product NDC: | 16590-071 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077749 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060331 |
Package Information of DIAZEPAM
| Package NDC: | 16590-071-75 |
| Package Description: | 75 TABLET in 1 BOTTLE (16590-071-75) |
NDC Information of DIAZEPAM
| NDC Code | 16590-071-75 |
| Proprietary Name | DIAZEPAM |
| Package Description | 75 TABLET in 1 BOTTLE (16590-071-75) |
| Product NDC | 16590-071 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DIAZEPAM |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20060331 |
| Marketing Category Name | ANDA |
| Labeler Name | STAT RX USA LLC |
| Substance Name | DIAZEPAM |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
