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"69953-515-01" National Drug Code (NDC)

Morning After 1 BLISTER PACK in 1 CARTON (69953-515-01) > 1 mg in 1 BLISTER PACK
(Rapha Pharmaceuticals, Inc.)

NDC Code69953-515-01
Package Description1 BLISTER PACK in 1 CARTON (69953-515-01) > 1 mg in 1 BLISTER PACK
Product NDC69953-515
Product Type NameHUMAN OTC DRUG
Proprietary NameMorning After
Non-Proprietary NameLevonorgestrel
Dosage FormTABLET
UsageORAL
Start Marketing Date20180322
Marketing Category NameANDA
Application NumberANDA206867
ManufacturerRapha Pharmaceuticals, Inc.
Substance NameLEVONORGESTREL
Strength1.5
Strength Unitmg/1.5mg
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/69953-515-01





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