Details for New Drug Application (NDA): 078786
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NDA 078786 describes CARVEDILOL, which is a drug marketed by Aurobindo Pharma, Chartwell Molecular, Glenmark Pharms Ltd, Hikma, Lupin, MLV, Pliva Hrvatska Doo, Regcon Holdings, Rising, Rubicon Research, Sandoz, Sciegen Pharms, Sun Pharm Inds Inc, Sun Pharm Inds Ltd, Taro, Teva, Zydus Pharms Usa Inc, Impax Labs Inc, and Sun Pharm Industries, and is included in nineteen NDAs. It is available from thirty-six suppliers. Additional details are available on the CARVEDILOL profile page.
The generic ingredient in CARVEDILOL is carvedilol phosphate. There are two drug master file entries for this compound. Nine suppliers are listed for this compound. Additional details are available on the carvedilol phosphate profile page.
The generic ingredient in CARVEDILOL is carvedilol phosphate. There are two drug master file entries for this compound. Nine suppliers are listed for this compound. Additional details are available on the carvedilol phosphate profile page.
Summary for 078786
| Tradename: | CARVEDILOL |
| Applicant: | Mlv |
| Ingredient: | carvedilol |
| Patents: | 0 |
Pharmacology for NDA: 078786
| Mechanism of Action | Adrenergic alpha-Antagonists Adrenergic beta1-Antagonists Adrenergic beta2-Antagonists |
Suppliers and Packaging for NDA: 078786
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| CARVEDILOL | carvedilol | TABLET;ORAL | 078786 | ANDA | Method Pharmaceuticals, LLC | 58657-750 | 58657-750-01 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (58657-750-01) |
| CARVEDILOL | carvedilol | TABLET;ORAL | 078786 | ANDA | Method Pharmaceuticals, LLC | 58657-750 | 58657-750-50 | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (58657-750-50) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 3.125MG | ||||
| Approval Date: | Dec 22, 2009 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 6.25MG | ||||
| Approval Date: | Dec 22, 2009 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 12.5MG | ||||
| Approval Date: | Dec 22, 2009 | TE: | AB | RLD: | No | ||||
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