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KLONOPIN
KLONOPIN - 16590-693-56 - (CLONAZEPAM)
Drug Information of KLONOPIN
| Product NDC: | 16590-693 |
| Proprietary Name: | KLONOPIN |
| Non Proprietary Name: | CLONAZEPAM |
| Active Ingredient(s): | .5 mg/1 & nbsp; CLONAZEPAM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of KLONOPIN
| Product NDC: | 16590-693 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA017533 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19750602 |
Package Information of KLONOPIN
| Package NDC: | 16590-693-56 |
| Package Description: | 56 TABLET in 1 BOTTLE (16590-693-56) |
NDC Information of KLONOPIN
| NDC Code | 16590-693-56 |
| Proprietary Name | KLONOPIN |
| Package Description | 56 TABLET in 1 BOTTLE (16590-693-56) |
| Product NDC | 16590-693 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CLONAZEPAM |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19750602 |
| Marketing Category Name | NDA |
| Labeler Name | STAT RX USA LLC |
| Substance Name | CLONAZEPAM |
| Strength Number | .5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
