Details for New Drug Application (NDA): 077321
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The generic ingredient in LISINOPRIL is hydrochlorothiazide; lisinopril. There are thirty-two drug master file entries for this compound. Thirty-four suppliers are listed for this compound. Additional details are available on the hydrochlorothiazide; lisinopril profile page.
Summary for 077321
Tradename: | LISINOPRIL |
Applicant: | Lupin |
Ingredient: | lisinopril |
Patents: | 0 |
Pharmacology for NDA: 077321
Mechanism of Action | Angiotensin-converting Enzyme Inhibitors |
Medical Subject Heading (MeSH) Categories for 077321
Suppliers and Packaging for NDA: 077321
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
LISINOPRIL | lisinopril | TABLET;ORAL | 077321 | ANDA | NCS HealthCare of KY, LLC dba Vangard Labs | 0615-8252 | 0615-8252-05 | 15 TABLET in 1 BLISTER PACK (0615-8252-05) |
LISINOPRIL | lisinopril | TABLET;ORAL | 077321 | ANDA | NCS HealthCare of KY, LLC dba Vangard Labs | 0615-8252 | 0615-8252-39 | 30 TABLET in 1 BLISTER PACK (0615-8252-39) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 2.5MG | ||||
Approval Date: | Sep 9, 2005 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 5MG | ||||
Approval Date: | Sep 9, 2005 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 10MG | ||||
Approval Date: | Sep 9, 2005 | TE: | AB | RLD: | No |
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