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"0603-7512-49" National Drug Code (NDC)

Kimidess 3 BLISTER PACK in 1 CARTON (0603-7512-49) > 1 KIT in 1 BLISTER PACK (0603-7512-01) * 21 TABLET, FILM COATED in 1 BLISTER PACK * 5 TABLET, FILM COATED in 1 BLISTER PACK
(Par Pharmaceutical)

NDC Code0603-7512-49
Package Description3 BLISTER PACK in 1 CARTON (0603-7512-49) > 1 KIT in 1 BLISTER PACK (0603-7512-01) * 21 TABLET, FILM COATED in 1 BLISTER PACK * 5 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC0603-7512
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameKimidess
Non-Proprietary NameDesogestrel And Ethinyl Estradiol
Dosage FormKIT
Start Marketing Date20150608
End Marketing Date20210131
Marketing Category NameANDA
Application NumberANDA076681
ManufacturerPar Pharmaceutical

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