Details for New Drug Application (NDA): 076007
✉ Email this page to a colleague
The generic ingredient in LISINOPRIL AND HYDROCHLOROTHIAZIDE is hydrochlorothiazide; lisinopril. There are thirty-two drug master file entries for this compound. Twenty-eight suppliers are listed for this compound. Additional details are available on the hydrochlorothiazide; lisinopril profile page.
Summary for 076007
| Tradename: | LISINOPRIL AND HYDROCHLOROTHIAZIDE |
| Applicant: | Sun Pharm Inds Ltd |
| Ingredient: | hydrochlorothiazide; lisinopril |
| Patents: | 0 |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 12.5MG;10MG | ||||
| Approval Date: | Jul 1, 2002 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 12.5MG;20MG | ||||
| Approval Date: | Jul 1, 2002 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 25MG;20MG | ||||
| Approval Date: | Jul 1, 2002 | TE: | AB | RLD: | No | ||||
Complete Access Available with Subscription
