USFDA APPLICATION NUMBER - 19851 / DOSAGE - TABLET;ORAL - 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Active Ingredient/Active Moiety | ||
Ingredient Name | Basis of Strength | Strength |
---|---|---|
BENAZEPRIL HYDROCHLORIDE(UNII: N1SN99T69T) (BENAZEPRILAT - UNII:JRM708L703) | BENAZEPRIL HYDROCHLORIDE | 20mg |
Inactive Ingredients
Ingredient Name | PD-Rx Pharmaceuticals, Inc. |
---|---|
CELLULOSE, MICROCRYSTALLINE(OP1R32D61U) | |
CROSPOVIDONE(68401960MK) | |
HYDROGENATED CASTOR OIL(ZF94AP8MEY) | |
HYPROMELLOSES(3NXW29V3WO) | |
LACTOSE(J2B2A4N98G) | |
POLYSORBATE 80(6OZP39ZG8H) | |
SILICON DIOXIDE(ETJ7Z6XBU4) | |
STARCH, POTATO(8I089SAH3T) | |
TALC(7SEV7J4R1U) | |
TITANIUM DIOXIDE(15FIX9V2JP) |
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