"50458-707-14" National Drug Code (NDC)

NDC Code	50458-707-14
Package Description	1 KIT in 1 CARTON (50458-707-14) * 1 BLISTER PACK in 1 CARTON (50458-706-00) / 1 TABLET, FILM COATED in 1 BLISTER PACK * 1 BLISTER PACK in 1 CARTON (50458-709-00) / 1 TABLET, FILM COATED in 1 BLISTER PACK * 1 BLISTER PACK in 1 CARTON (50458-708-00) / 1 TABLET, FILM COATED in 1 BLISTER PACK * 1 BLISTER PACK in 1 CARTON (50458-711-00) / 1 TABLET, FILM COATED in 1 BLISTER PACK * 1 BLISTER PACK in 1 CARTON (50458-710-00) / 3 TABLET, FILM COATED in 1 BLISTER PACK * 1 BLISTER PACK in 1 CARTON (50458-705-00) / 1 TABLET, FILM COATED in 1 BLISTER PACK * 1 BLISTER PACK in 1 CARTON (50458-704-00) / 2 TABLET, FILM COATED in 1 BLISTER PACK * 1 BLISTER PACK in 1 CARTON (50458-703-00) / 2 TABLET, FILM COATED in 1 BLISTER PACK * 1 BLISTER PACK in 1 CARTON (50458-702-00) / 2 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC	50458-707
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Ponvory
Non-Proprietary Name	Ponesimod
Dosage Form	KIT
Start Marketing Date	20210318
End Marketing Date	20270331
Marketing Category Name	NDA
Application Number	NDA213498
Manufacturer	Janssen Pharmaceuticals, Inc.