Details for New Drug Application (NDA): 211033
✉ Email this page to a colleague
NDA 211033 describes CLONAZEPAM, which is a drug marketed by Alembic, Barr, Endo Operations, Sun Pharm Inds Inc, Accord Hlthcare, Actavis Elizabeth, Aurobindo Pharma Usa, Chartwell Rx, Norvium Bioscience, Prinston Inc, Rubicon, Sandoz, Teva, and Watson Labs, and is included in sixteen NDAs. It is available from thirty-two suppliers. Additional details are available on the CLONAZEPAM profile page.
The generic ingredient in CLONAZEPAM is clonazepam. There are ten drug master file entries for this compound. Thirty-three suppliers are listed for this compound. Additional details are available on the clonazepam profile page.
The generic ingredient in CLONAZEPAM is clonazepam. There are ten drug master file entries for this compound. Thirty-three suppliers are listed for this compound. Additional details are available on the clonazepam profile page.
Summary for 211033
| Tradename: | CLONAZEPAM |
| Applicant: | Alembic |
| Ingredient: | clonazepam |
| Patents: | 0 |
Suppliers and Packaging for NDA: 211033
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| CLONAZEPAM | clonazepam | TABLET, ORALLY DISINTEGRATING;ORAL | 211033 | ANDA | Alembic Pharmaceuticals Limited | 46708-364 | 46708-364-06 | 60 BLISTER PACK in 1 CARTON (46708-364-06) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
| CLONAZEPAM | clonazepam | TABLET, ORALLY DISINTEGRATING;ORAL | 211033 | ANDA | Alembic Pharmaceuticals Limited | 46708-365 | 46708-365-06 | 60 BLISTER PACK in 1 CARTON (46708-365-06) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, ORALLY DISINTEGRATING;ORAL | Strength | 0.125MG | ||||
| Approval Date: | Jun 28, 2019 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, ORALLY DISINTEGRATING;ORAL | Strength | 0.25MG | ||||
| Approval Date: | Jun 28, 2019 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, ORALLY DISINTEGRATING;ORAL | Strength | 0.5MG | ||||
| Approval Date: | Jun 28, 2019 | TE: | AB | RLD: | No | ||||
Complete Access Available with Subscription
