Details for New Drug Application (NDA): 076007
NDA 076007 describes LISINOPRIL AND HYDROCHLOROTHIAZIDE, which is a drug marketed by Aiping Pharm Inc, Aurobindo, Chartwell Rx, Epic Pharma Llc, Hikma, Invagen Pharms, Lupin, Macleods Pharms, Pharmobedient, Prinston Inc, Sun Pharm Inds Ltd, Teva, and Watson Labs, and is included in thirteen NDAs. It is available from twenty-seven suppliers. Additional details are available on the LISINOPRIL AND HYDROCHLOROTHIAZIDE profile page.
The generic ingredient in LISINOPRIL AND HYDROCHLOROTHIAZIDE is hydrochlorothiazide; lisinopril. There is one drug master file entry for this compound. Twenty-eight suppliers are listed for this compound. Additional details are available on the hydrochlorothiazide; lisinopril profile page.
The generic ingredient in LISINOPRIL AND HYDROCHLOROTHIAZIDE is hydrochlorothiazide; lisinopril. There is one drug master file entry 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 | ||||
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