"50102-220-23" National Drug Code (NDC)

Aubra Eq 3 POUCH in 1 CARTON (50102-220-23) / 1 BLISTER PACK in 1 POUCH (50102-220-21) / 1 KIT in 1 BLISTER PACK
(Afaxys Pharma, LLC)

NDC Code50102-220-23
Package Description3 POUCH in 1 CARTON (50102-220-23) / 1 BLISTER PACK in 1 POUCH (50102-220-21) / 1 KIT in 1 BLISTER PACK
Product NDC50102-220
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAubra Eq
Non-Proprietary NameLevonorgestrel And Ethinyl Estradiol
Dosage FormKIT
Start Marketing Date20161114
Marketing Category NameANDA
Application NumberANDA206886
ManufacturerAfaxys Pharma, LLC

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