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USFDA APPLICATION NUMBER - 18063 / DOSAGE - TABLET;ORAL - 80MG
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| NADOLOL(UNII: FEN504330V) (NADOLOL - UNII:FEN504330V) | NADOLOL | 80mg | 40mg | 20mg |
Inactive Ingredients
| Ingredient Name | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | Teva Pharmaceuticals USA, Inc. | Bryant Ranch Prepack | Mylan Institutional Inc. | American Health Packaging | Avera McKennan Hospital | BluePoint Laboratories | Ingenus Pharmaceuticals, LLC | Sandoz Inc | US WorldMeds, LLC |
|---|---|---|---|---|---|---|---|---|---|---|
| ANHYDROUS CITRIC ACID(XF417D3PSL) | ||||||||||
| ANHYDROUS LACTOSE(3SY5LH9PMK) | ||||||||||
| CELLULOSE, MICROCRYSTALLINE(OP1R32D61U) | ||||||||||
| CROSCARMELLOSE SODIUM(M28OL1HH48) | ||||||||||
| D&C YELLOW NO. 10(35SW5USQ3G) | ||||||||||
| FD&C BLUE NO. 2(L06K8R7DQK) | ||||||||||
| HYDROXYPROPYL CELLULOSE (1200000 MW)(RFW2ET671P) | ||||||||||
| HYDROXYPROPYL CELLULOSE (TYPE H)(RFW2ET671P) | ||||||||||
| HYDROXYPROPYL CELLULOSE (TYPE M)(U3JF91U133) | ||||||||||
| LACTOSE MONOHYDRATE(EWQ57Q8I5X) | ||||||||||
| MAGNESIUM STEARATE(70097M6I30) | ||||||||||
| MICROCRYSTALLINE CELLULOSE(OP1R32D61U) | ||||||||||
| POVIDONE K30(U725QWY32X) | ||||||||||
| POVIDONE, UNSPECIFIED(FZ989GH94E) | ||||||||||
| SILICON DIOXIDE(ETJ7Z6XBU4) | ||||||||||
| SODIUM LAURYL SULFATE(368GB5141J) | ||||||||||
| SODIUM STARCH GLYCOLATE TYPE A POTATO(5856J3G2A2) | ||||||||||
| SODIUM STARCH GLYCOLATE TYPE A(H8AV0SQX4D) | ||||||||||
| STARCH, CORN(O8232NY3SJ) | ||||||||||
| WATER(059QF0KO0R) |
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