Details for New Drug Application (NDA): 075903
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NDA 075903 describes LISINOPRIL, which is a drug marketed by Accord Hlthcare, Ascent Pharms Inc, Aurobindo, Chartwell Rx, Corepharma, Heritage Pharma, Hikma Intl Pharms, Invagen Pharms, Lupin, Prinston Inc, Rising, Sciegen Pharms Inc, Strides Pharma, Sun Pharm Inds Ltd, Teva, Watson Labs, Wockhardt Bio Ag, Epic Pharma Llc, Norvium Bioscience, and Sandoz, and is included in thirty-two NDAs. It is available from forty-two suppliers. Additional details are available on the LISINOPRIL profile page.
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.
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 075903
| Tradename: | LISINOPRIL |
| Applicant: | Ascent Pharms Inc |
| Ingredient: | lisinopril |
| Patents: | 0 |
Pharmacology for NDA: 075903
| Mechanism of Action | Angiotensin-converting Enzyme Inhibitors |
Medical Subject Heading (MeSH) Categories for 075903
Suppliers and Packaging for NDA: 075903
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| LISINOPRIL | lisinopril | TABLET;ORAL | 075903 | ANDA | Camber Pharmaceuticals, Inc. | 31722-172 | 31722-172-31 | 95238 TABLET in 1 CARTON (31722-172-31) |
| LISINOPRIL | lisinopril | TABLET;ORAL | 075903 | ANDA | Camber Pharmaceuticals, Inc. | 31722-172 | 31722-172-01 | 100 TABLET in 1 BOTTLE (31722-172-01) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 2.5MG | ||||
| Approval Date: | Jul 1, 2002 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 5MG | ||||
| Approval Date: | Jul 1, 2002 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 10MG | ||||
| Approval Date: | Jul 1, 2002 | TE: | AB | RLD: | No | ||||
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