Details for New Drug Application (NDA): 076204
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The generic ingredient in MOEXIPRIL HYDROCHLORIDE is hydrochlorothiazide; moexipril hydrochloride. There are thirty-two drug master file entries for this compound. Additional details are available on the hydrochlorothiazide; moexipril hydrochloride profile page.
Summary for 076204
Tradename: | MOEXIPRIL HYDROCHLORIDE |
Applicant: | Teva |
Ingredient: | moexipril hydrochloride |
Patents: | 0 |
Pharmacology for NDA: 076204
Mechanism of Action | Angiotensin-converting Enzyme Inhibitors |
Suppliers and Packaging for NDA: 076204
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
MOEXIPRIL HYDROCHLORIDE | moexipril hydrochloride | TABLET;ORAL | 076204 | ANDA | Teva Pharmaceuticals USA, Inc. | 0093-0017 | 0093-0017-01 | 100 TABLET, FILM COATED in 1 BOTTLE (0093-0017-01) |
MOEXIPRIL HYDROCHLORIDE | moexipril hydrochloride | TABLET;ORAL | 076204 | ANDA | Teva Pharmaceuticals USA, Inc. | 0093-5150 | 0093-5150-01 | 100 TABLET, FILM COATED in 1 BOTTLE (0093-5150-01) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 7.5MG | ||||
Approval Date: | May 8, 2003 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 15MG | ||||
Approval Date: | May 8, 2003 | TE: | AB | RLD: | No |
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