Details for New Drug Application (NDA): 078245
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The generic ingredient in LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE is hydrochlorothiazide; losartan potassium. There are thirty-two drug master file entries for this compound. Thirty suppliers are listed for this compound. Additional details are available on the hydrochlorothiazide; losartan potassium profile page.
Summary for 078245
| Tradename: | LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE |
| Applicant: | Lupin Ltd |
| Ingredient: | hydrochlorothiazide; losartan potassium |
| Patents: | 0 |
Pharmacology for NDA: 078245
| Mechanism of Action | Angiotensin 2 Receptor Antagonists |
| Physiological Effect | Increased Diuresis |
Suppliers and Packaging for NDA: 078245
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE | hydrochlorothiazide; losartan potassium | TABLET;ORAL | 078245 | ANDA | A-S Medication Solutions | 50090-4993 | 50090-4993-0 | 30 TABLET in 1 BOTTLE (50090-4993-0) |
| LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE | hydrochlorothiazide; losartan potassium | TABLET;ORAL | 078245 | ANDA | A-S Medication Solutions | 50090-4993 | 50090-4993-1 | 90 TABLET in 1 BOTTLE (50090-4993-1) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 12.5MG;50MG | ||||
| Approval Date: | Oct 6, 2010 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 12.5MG;100MG | ||||
| Approval Date: | May 21, 2010 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 25MG;100MG | ||||
| Approval Date: | Oct 6, 2010 | TE: | AB | RLD: | No | ||||
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