Details for New Drug Application (NDA): 020757
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The generic ingredient in AVAPRO is irbesartan. There are thirty-eight drug master file entries for this compound. Twenty-four suppliers are listed for this compound. Additional details are available on the irbesartan profile page.
Summary for 020757
| Tradename: | AVAPRO |
| Applicant: | Sanofi Aventis Us |
| Ingredient: | irbesartan |
| Patents: | 0 |
Pharmacology for NDA: 020757
| Mechanism of Action | Angiotensin 2 Receptor Antagonists |
Suppliers and Packaging for NDA: 020757
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| AVAPRO | irbesartan | TABLET;ORAL | 020757 | NDA | Sanofi-Aventis U.S. LLC | 0024-5851 | 0024-5851-30 | 30 TABLET, FILM COATED in 1 BOTTLE (0024-5851-30) |
| AVAPRO | irbesartan | TABLET;ORAL | 020757 | NDA | Sanofi-Aventis U.S. LLC | 0024-5852 | 0024-5852-30 | 30 TABLET, FILM COATED in 1 BOTTLE (0024-5852-30) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 75MG | ||||
| Approval Date: | Sep 30, 1997 | TE: | RLD: | Yes | |||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 150MG | ||||
| Approval Date: | Sep 30, 1997 | TE: | AB | RLD: | Yes | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 300MG | ||||
| Approval Date: | Sep 30, 1997 | TE: | AB | RLD: | Yes | ||||
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