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TEMAZEPAM
TEMAZEPAM - 68084-549-21 - (temazepam)
Drug Information of TEMAZEPAM
| Product NDC: | 68084-549 |
| Proprietary Name: | TEMAZEPAM |
| Non Proprietary Name: | temazepam |
| Active Ingredient(s): | 7.5 mg/1 & nbsp; temazepam |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TEMAZEPAM
| Product NDC: | 68084-549 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018163 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120201 |
Package Information of TEMAZEPAM
| Package NDC: | 68084-549-21 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (68084-549-21) > 10 CAPSULE in 1 BLISTER PACK (68084-549-11) (68084-549-11) |
NDC Information of TEMAZEPAM
| NDC Code | 68084-549-21 |
| Proprietary Name | TEMAZEPAM |
| Package Description | 3 BLISTER PACK in 1 CARTON (68084-549-21) > 10 CAPSULE in 1 BLISTER PACK (68084-549-11) (68084-549-11) |
| Product NDC | 68084-549 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | temazepam |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20120201 |
| Marketing Category Name | NDA |
| Labeler Name | American Health Packaging |
| Substance Name | TEMAZEPAM |
| Strength Number | 7.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
