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temazepam
temazepam - 21695-282-78 - (temazepam)
Drug Information of temazepam
| Product NDC: | 21695-282 |
| Proprietary Name: | temazepam |
| Non Proprietary Name: | temazepam |
| Active Ingredient(s): | 15 mg/1 & nbsp; temazepam |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of temazepam
| Product NDC: | 21695-282 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA071456 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19870421 |
Package Information of temazepam
| Package NDC: | 21695-282-78 |
| Package Description: | 180 CAPSULE in 1 BOTTLE (21695-282-78) |
NDC Information of temazepam
| NDC Code | 21695-282-78 |
| Proprietary Name | temazepam |
| Package Description | 180 CAPSULE in 1 BOTTLE (21695-282-78) |
| Product NDC | 21695-282 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | temazepam |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19870421 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | TEMAZEPAM |
| Strength Number | 15 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
