Details for New Drug Application (NDA): 077171
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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 077171
Tradename: | CLONAZEPAM |
Applicant: | Endo Operations |
Ingredient: | clonazepam |
Patents: | 0 |
Suppliers and Packaging for NDA: 077171
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
CLONAZEPAM | clonazepam | TABLET, ORALLY DISINTEGRATING;ORAL | 077171 | ANDA | Par Pharmaceutical, Inc. | 49884-306 | 49884-306-02 | 60 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (49884-306-02) |
CLONAZEPAM | clonazepam | TABLET, ORALLY DISINTEGRATING;ORAL | 077171 | ANDA | Par Pharmaceutical, Inc. | 49884-307 | 49884-307-02 | 60 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (49884-307-02) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, ORALLY DISINTEGRATING;ORAL | Strength | 0.125MG | ||||
Approval Date: | Aug 3, 2005 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, ORALLY DISINTEGRATING;ORAL | Strength | 0.25MG | ||||
Approval Date: | Aug 3, 2005 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET, ORALLY DISINTEGRATING;ORAL | Strength | 0.5MG | ||||
Approval Date: | Aug 3, 2005 | TE: | AB | RLD: | No |
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