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Clonazepam
Clonazepam - 49884-309-02 - (clonazepam)
Drug Information of Clonazepam
| Product NDC: | 49884-309 |
| Proprietary Name: | Clonazepam |
| Non Proprietary Name: | clonazepam |
| Active Ingredient(s): | 1 mg/1 & nbsp; clonazepam |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Clonazepam
| Product NDC: | 49884-309 |
| Labeler Name: | Par Pharmaceutical, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077171 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050805 |
Package Information of Clonazepam
| Package NDC: | 49884-309-02 |
| Package Description: | 60 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (49884-309-02) |
NDC Information of Clonazepam
| NDC Code | 49884-309-02 |
| Proprietary Name | Clonazepam |
| Package Description | 60 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (49884-309-02) |
| Product NDC | 49884-309 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | clonazepam |
| Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
| Route Name | ORAL |
| Start Marketing Date | 20050805 |
| Marketing Category Name | ANDA |
| Labeler Name | Par Pharmaceutical, Inc. |
| Substance Name | CLONAZEPAM |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
