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Diazepam
Diazepam - 17856-3188-2 - (Diazepam)
Drug Information of Diazepam
| Product NDC: | 17856-3188 |
| Proprietary Name: | Diazepam |
| Non Proprietary Name: | Diazepam |
| Active Ingredient(s): | 5 mg/5mL & nbsp; Diazepam |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Diazepam
| Product NDC: | 17856-3188 |
| Labeler Name: | Atlantic Biologicals Corps |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA070928 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19870403 |
Package Information of Diazepam
| Package NDC: | 17856-3188-2 |
| Package Description: | 2 mL in 1 CUP (17856-3188-2) |
NDC Information of Diazepam
| NDC Code | 17856-3188-2 |
| Proprietary Name | Diazepam |
| Package Description | 2 mL in 1 CUP (17856-3188-2) |
| Product NDC | 17856-3188 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Diazepam |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 19870403 |
| Marketing Category Name | ANDA |
| Labeler Name | Atlantic Biologicals Corps |
| Substance Name | DIAZEPAM |
| Strength Number | 5 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
