"0555-9019-57" National Drug Code (NDC)

NDC Code	0555-9019-57
Package Description	6 BLISTER PACK in 1 CARTON (0555-9019-57) > 21 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC	0555-9019
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Portia
Non-Proprietary Name	Levonorgestrel And Ethinyl Estradiol
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20020627
Marketing Category Name	ANDA
Application Number	ANDA075866
Manufacturer	Barr Laboratories Inc.
Substance Name	ETHINYL ESTRADIOL; LEVONORGESTREL
Strength	.03; .15
Strength Unit	mg/1; mg/1
Pharmacy Classes	Estrogen [EPC],Estrogen Receptor Agonists [MoA],Inhibit Ovum Fertilization [PE],Progesterone Congeners [Chemical/Ingredient],Progesterone Congeners [Chemical/Ingredient],Progestin [EPC],Progestin-containing Intrauterine Device [EPC]