USFDA APPLICATION NUMBER - 18716 / DOSAGE - TABLET;ORAL - 400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
---|---|---|
labetalol hydrochloride(UNII: 1GEV3BAW9J) (labetalol - UNII:R5H8897N95) | labetalol hydrochloride | 300mg | 200mg | 100mg |
Inactive Ingredients
Ingredient Name | Alvogen Inc. | Bryant Ranch Prepack | County Line Pharmaceuticals LLC | NuCare Pharmaceuticals, Inc. | REMEDYREPACK INC. | St. Mary's Medical Park Pharmacy | A-S Medication Solutions |
---|---|---|---|---|---|---|---|
FD&C YELLOW NO. 6(H77VEI93A8) | |||||||
HYPROMELLOSE 2910 (6 MPA.S)(0WZ8WG20P6) | |||||||
lactose, unspecified form(J2B2A4N98G) | |||||||
magnesium stearate(70097M6I30) | |||||||
SODIUM BENZOATE(OJ245FE5EU) | |||||||
STARCH, CORN(O8232NY3SJ) | |||||||
TALC(7SEV7J4R1U) | |||||||
TITANIUM DIOXIDE(15FIX9V2JP) |
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