
USFDA APPLICATION NUMBER - 18647 / DOSAGE - TABLET;ORAL - 5MG;80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
|---|---|---|
| BENDROFLUMETHIAZIDE(UNII: 5Q52X6ICJI) (BENDROFLUMETHIAZIDE - UNII:5Q52X6ICJI) | BENDROFLUMETHIAZIDE | 5mg | 5mg |
| NADOLOL(UNII: FEN504330V) (NADOLOL - UNII:FEN504330V) | NADOLOL | 40mg | 80mg |
Inactive Ingredients
| Ingredient Name | Pfizer Laboratories Div Pfizer Inc |
|---|---|
| FD&C BLUE NO. 2(L06K8R7DQK) | |
| LACTOSE, UNSPECIFIED FORM(J2B2A4N98G) | |
| MAGNESIUM STEARATE(70097M6I30) | |
| MICROCRYSTALLINE CELLULOSE(OP1R32D61U) | |
| POVIDONE, UNSPECIFIED(FZ989GH94E) | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO(5856J3G2A2) |