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temazepam
temazepam - 67877-149-01 - (temazepam)
Drug Information of temazepam
| Product NDC: | 67877-149 |
| Proprietary Name: | temazepam |
| Non Proprietary Name: | temazepam |
| Active Ingredient(s): | 22.5 mg/1 & nbsp; temazepam |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of temazepam
| Product NDC: | 67877-149 |
| Labeler Name: | Ascend Laboratories, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA071457 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120628 |
Package Information of temazepam
| Package NDC: | 67877-149-01 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (67877-149-01) |
NDC Information of temazepam
| NDC Code | 67877-149-01 |
| Proprietary Name | temazepam |
| Package Description | 100 CAPSULE in 1 BOTTLE (67877-149-01) |
| Product NDC | 67877-149 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | temazepam |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20120628 |
| Marketing Category Name | ANDA |
| Labeler Name | Ascend Laboratories, LLC |
| Substance Name | TEMAZEPAM |
| Strength Number | 22.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
