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Diazepam
Diazepam - 0093-6138-32 - (Diazepam)
Drug Information of Diazepam
| Product NDC: | 0093-6138 |
| Proprietary Name: | Diazepam |
| Non Proprietary Name: | Diazepam |
| Active Ingredient(s): | 10 mg/2mL & nbsp; Diazepam |
| Administration Route(s): | RECTAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Diazepam
| Product NDC: | 0093-6138 |
| Labeler Name: | Teva Pharmaceuticals USA Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020648 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20100903 |
Package Information of Diazepam
| Package NDC: | 0093-6138-32 |
| Package Description: | 2 SYRINGE, PLASTIC in 1 PACKAGE (0093-6138-32) > 2 mL in 1 SYRINGE, PLASTIC |
NDC Information of Diazepam
| NDC Code | 0093-6138-32 |
| Proprietary Name | Diazepam |
| Package Description | 2 SYRINGE, PLASTIC in 1 PACKAGE (0093-6138-32) > 2 mL in 1 SYRINGE, PLASTIC |
| Product NDC | 0093-6138 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Diazepam |
| Dosage Form Name | GEL |
| Route Name | RECTAL |
| Start Marketing Date | 20100903 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Teva Pharmaceuticals USA Inc |
| Substance Name | DIAZEPAM |
| Strength Number | 10 |
| Strength Unit | mg/2mL |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
