Details for New Drug Application (NDA): 077622
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The generic ingredient in LISINOPRIL is hydrochlorothiazide; lisinopril. There are thirty-two drug master file entries for this compound. Thirty-three suppliers are listed for this compound. Additional details are available on the hydrochlorothiazide; lisinopril profile page.
Summary for 077622
Tradename: | LISINOPRIL |
Applicant: | Aurobindo |
Ingredient: | lisinopril |
Patents: | 0 |
Formulation / Manufacturing: | see details |
Pharmacology for NDA: 077622
Mechanism of Action | Angiotensin-converting Enzyme Inhibitors |
Medical Subject Heading (MeSH) Categories for 077622
Suppliers and Packaging for NDA: 077622
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
LISINOPRIL | lisinopril | TABLET;ORAL | 077622 | ANDA | Aurobindo Pharma Limited | 65862-037 | 65862-037-00 | 100 TABLET in 1 BOTTLE (65862-037-00) |
LISINOPRIL | lisinopril | TABLET;ORAL | 077622 | ANDA | Aurobindo Pharma Limited | 65862-037 | 65862-037-01 | 100 TABLET in 1 BOTTLE (65862-037-01) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 2.5MG | ||||
Approval Date: | Feb 22, 2006 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 5MG | ||||
Approval Date: | Feb 22, 2006 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 10MG | ||||
Approval Date: | Feb 22, 2006 | TE: | AB | RLD: | No |
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