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"58602-712-28" National Drug Code (NDC)

Fem Choice Morning After 1 BLISTER PACK in 1 CARTON (58602-712-28) / 1 TABLET in 1 BLISTER PACK
(Aurohealth LLC)

NDC Code58602-712-28
Package Description1 BLISTER PACK in 1 CARTON (58602-712-28) / 1 TABLET in 1 BLISTER PACK
Product NDC58602-712
Product Type NameHUMAN OTC DRUG
Proprietary NameFem Choice Morning After
Non-Proprietary NameLevonorgestrel
Dosage FormTABLET
UsageORAL
Start Marketing Date20220126
Marketing Category NameANDA
Application NumberANDA206867
ManufacturerAurohealth LLC
Substance NameLEVONORGESTREL
Strength1.5
Strength Unitmg/1
Pharmacy ClassesInhibit Ovum Fertilization [PE], Progesterone Congeners [CS], Progesterone Congeners [CS], Progestin [EPC], Progestin-containing Intrauterine Device [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/58602-712-28





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