Details for New Drug Application (NDA): 075731
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NDA 075731 describes CLORAZEPATE DIPOTASSIUM, which is a drug marketed by Able, Am Therap, Dash Pharms, Dava Pharms Inc, Gd Searle Llc, Purepac Pharm, Quantum Pharmics, Rising, Usl Pharma, Warner Chilcott, Watson Labs, Aurobindo Pharma, Aurolife Pharma Llc, Corepharma, Lederle, Novitium Pharma, Sun Pharm Inds Ltd, and Taro, and is included in fifty-eight NDAs. It is available from seven suppliers. Additional details are available on the CLORAZEPATE DIPOTASSIUM profile page.
The generic ingredient in CLORAZEPATE DIPOTASSIUM is clorazepate dipotassium. There are eight drug master file entries for this compound. Seven suppliers are listed for this compound. Additional details are available on the clorazepate dipotassium profile page.
The generic ingredient in CLORAZEPATE DIPOTASSIUM is clorazepate dipotassium. There are eight drug master file entries for this compound. Seven suppliers are listed for this compound. Additional details are available on the clorazepate dipotassium profile page.
Summary for 075731
| Tradename: | CLORAZEPATE DIPOTASSIUM |
| Applicant: | Taro |
| Ingredient: | clorazepate dipotassium |
| Patents: | 0 |
Suppliers and Packaging for NDA: 075731
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| CLORAZEPATE DIPOTASSIUM | clorazepate dipotassium | TABLET;ORAL | 075731 | ANDA | PD-Rx Pharmaceuticals, Inc. | 43063-893 | 43063-893-06 | 6 TABLET in 1 BOTTLE, PLASTIC (43063-893-06) |
| CLORAZEPATE DIPOTASSIUM | clorazepate dipotassium | TABLET;ORAL | 075731 | ANDA | Taro Pharmaceuticals U.S.A., Inc. | 51672-4042 | 51672-4042-1 | 100 TABLET in 1 BOTTLE (51672-4042-1) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 15MG | ||||
| Approval Date: | Apr 27, 2000 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 7.5MG | ||||
| Approval Date: | Apr 27, 2000 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 3.75MG | ||||
| Approval Date: | Apr 27, 2000 | TE: | AB | RLD: | No | ||||
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