Product NDC: | 68788-9940 |
Proprietary Name: | Clonazepam |
Non Proprietary Name: | Clonazepam |
Active Ingredient(s): | 1 mg/1 & nbsp; Clonazepam |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68788-9940 |
Labeler Name: | Preferred Pharmaceuticals, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA074869 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120117 |
Package NDC: | 68788-9940-2 |
Package Description: | 20 TABLET in 1 BOTTLE (68788-9940-2) |
NDC Code | 68788-9940-2 |
Proprietary Name | Clonazepam |
Package Description | 20 TABLET in 1 BOTTLE (68788-9940-2) |
Product NDC | 68788-9940 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Clonazepam |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20120117 |
Marketing Category Name | ANDA |
Labeler Name | Preferred Pharmaceuticals, Inc |
Substance Name | CLONAZEPAM |
Strength Number | 1 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |