Basic Information
Nebivolol
50090-5752
Regulatory Information
50090-5752
ANDA203828
C73584
April 13, 2022
USA
These highlights do not include all the information needed to use NEBIVOLOL TABLETS safely and effectively. See full prescribing information for NEBIVOLOL TABLETS. NEBIVOLOL tablets, for oral use Initial U.S. Approval: 2007
Human Prescription Drug Label
5
Company Information
830016429
Active Ingredients
Inactive Ingredients
CROSCARMELLOSE SODIUM
Code: M28OL1HH48
Class Code: IACT
FD&C YELLOW NO. 6
Code: H77VEI93A8
Class Code: IACT
SILICON DIOXIDE
Code: ETJ7Z6XBU4
Class Code: IACT
POLYETHYLENE GLYCOL 6000
Code: 30IQX730WE
Class Code: IACT
HYPROMELLOSE 2910 (15 MPA.S)
Code: 36SFW2JZ0W
Class Code: IACT
MICROCRYSTALLINE CELLULOSE
Code: OP1R32D61U
Class Code: IACT
MAGNESIUM STEARATE
Code: 70097M6I30
Class Code: IACT
STARCH, CORN
Code: O8232NY3SJ
Class Code: IACT
LACTOSE MONOHYDRATE
Code: EWQ57Q8I5X
Class Code: IACT
Active Moieties
NEBIVOLOL
Code: 030Y90569U