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Oxazepam
Oxazepam - 0781-2810-05 - (Oxazepam)
Drug Information of Oxazepam
| Product NDC: | 0781-2810 |
| Proprietary Name: | Oxazepam |
| Non Proprietary Name: | Oxazepam |
| Active Ingredient(s): | 15 mg/1 & nbsp; Oxazepam |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Oxazepam
| Product NDC: | 0781-2810 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA071756 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19880419 |
Package Information of Oxazepam
| Package NDC: | 0781-2810-05 |
| Package Description: | 500 CAPSULE in 1 BOTTLE (0781-2810-05) |
NDC Information of Oxazepam
| NDC Code | 0781-2810-05 |
| Proprietary Name | Oxazepam |
| Package Description | 500 CAPSULE in 1 BOTTLE (0781-2810-05) |
| Product NDC | 0781-2810 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Oxazepam |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19880419 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | OXAZEPAM |
| Strength Number | 15 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
