DrugPatentWatch Database Preview
Details for New Drug Application (NDA): 090382
The generic ingredient in LOSARTAN POTASSIUM is hydrochlorothiazide; losartan potassium. There are thirty-two drug master file entries for this compound. Thirty-nine suppliers are listed for this compound. Additional details are available on the hydrochlorothiazide; losartan potassium profile page.
Summary for 090382
Tradename: | LOSARTAN POTASSIUM |
Applicant: | Vivimed Global |
Ingredient: | losartan potassium |
Patents: | 0 |
Therapeutic Class: | Cardiovascular Agents |
Formulation / Manufacturing: | see details |
Pharmacology for NDA: 090382
Mechanism of Action | Angiotensin 2 Receptor Antagonists |
Medical Subject Heading (MeSH) Categories for 090382
Suppliers and Packaging for NDA: 090382
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
LOSARTAN POTASSIUM | losartan potassium | TABLET;ORAL | 090382 | ANDA | Heritage Pharmaceuticals Inc. | 23155-644 | N | 23155-644-09 |
LOSARTAN POTASSIUM | losartan potassium | TABLET;ORAL | 090382 | ANDA | Heritage Pharmaceuticals Inc. | 23155-644 | N | 23155-644-03 |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 25MG | ||||
Approval Date: | Oct 6, 2010 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 50MG | ||||
Approval Date: | Oct 6, 2010 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 100MG | ||||
Approval Date: | Oct 6, 2010 | TE: | AB | RLD: | No |
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