"69953-617-42" National Drug Code (NDC)

Postday One-step 1 BLISTER PACK in 1 CARTON (69953-617-42) / 1 mg in 1 BLISTER PACK
(Rapha Pharmaceuticals, Inc.)

NDC Code69953-617-42
Package Description1 BLISTER PACK in 1 CARTON (69953-617-42) / 1 mg in 1 BLISTER PACK
Product NDC69953-617
Product Type NameHUMAN OTC DRUG
Proprietary NamePostday One-step
Non-Proprietary NameLevonorgestrel
Dosage FormTABLET
UsageORAL
Start Marketing Date20230116
Marketing Category NameANDA
Application NumberANDA205329
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 System [EPC]

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