Details for New Drug Application (NDA): 219539
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The generic ingredient in IRBESARTAN is hydrochlorothiazide; irbesartan. There are thirty-two drug master file entries for this compound. Thirteen suppliers are listed for this compound. Additional details are available on the hydrochlorothiazide; irbesartan profile page.
Summary for 219539
| Tradename: | IRBESARTAN |
| Applicant: | Msn |
| Ingredient: | irbesartan |
| Patents: | 0 |
Pharmacology for NDA: 219539
| Mechanism of Action | Angiotensin 2 Receptor Antagonists |
Suppliers and Packaging for NDA: 219539
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| IRBESARTAN | irbesartan | TABLET;ORAL | 219539 | ANDA | Novadoz Pharmaceuticals LLC | 72205-327 | 72205-327-05 | 500 TABLET, FILM COATED in 1 BOTTLE (72205-327-05) |
| IRBESARTAN | irbesartan | TABLET;ORAL | 219539 | ANDA | Novadoz Pharmaceuticals LLC | 72205-327 | 72205-327-06 | 10 BLISTER PACK in 1 CARTON (72205-327-06) / 10 TABLET, FILM COATED in 1 BLISTER PACK |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 75MG | ||||
| Approval Date: | Nov 4, 2025 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 150MG | ||||
| Approval Date: | Nov 4, 2025 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 300MG | ||||
| Approval Date: | Nov 4, 2025 | TE: | AB | RLD: | No | ||||
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