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Temazepam
Temazepam - 76237-251-39 - (Temazepam)
Drug Information of Temazepam
| Product NDC: | 76237-251 |
| Proprietary Name: | Temazepam |
| Non Proprietary Name: | Temazepam |
| Active Ingredient(s): | 30 mg/1 & nbsp; Temazepam |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Temazepam
| Product NDC: | 76237-251 |
| Labeler Name: | McKesson Contract Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA071428 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111121 |
Package Information of Temazepam
| Package NDC: | 76237-251-39 |
| Package Description: | 30 CAPSULE in 1 BLISTER PACK (76237-251-39) |
NDC Information of Temazepam
| NDC Code | 76237-251-39 |
| Proprietary Name | Temazepam |
| Package Description | 30 CAPSULE in 1 BLISTER PACK (76237-251-39) |
| Product NDC | 76237-251 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Temazepam |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20111121 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson Contract Packaging |
| Substance Name | TEMAZEPAM |
| Strength Number | 30 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
