Product NDC: | 53489-648 |
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) |
Product NDC: | 53489-648 |
Labeler Name: | Mutual Pharmaceutical Company, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078581 |
Marketing Category: | ANDA |
Start Marketing Date: | 20090909 |
Package NDC: | 53489-648-07 |
Package Description: | 30 CAPSULE in 1 BOTTLE, PLASTIC (53489-648-07) |
NDC Code | 53489-648-07 |
Proprietary Name | Temazepam |
Package Description | 30 CAPSULE in 1 BOTTLE, PLASTIC (53489-648-07) |
Product NDC | 53489-648 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Temazepam |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20090909 |
Marketing Category Name | ANDA |
Labeler Name | Mutual Pharmaceutical Company, Inc. |
Substance Name | TEMAZEPAM |
Strength Number | 7.5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |