"51660-127-86" National Drug Code (NDC)

Norlyroc 1 BLISTER PACK in 1 CARTON (51660-127-86) > 28 TABLET, FILM COATED in 1 BLISTER PACK
(Ohm Laboratories Inc.)

NDC Code51660-127-86
Package Description1 BLISTER PACK in 1 CARTON (51660-127-86) > 28 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC51660-127
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNorlyroc
Non-Proprietary NameNorethindrone
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20140415
Marketing Category NameANDA
Application NumberANDA202260
ManufacturerOhm Laboratories Inc.
Substance NameNORETHINDRONE
Strength.35
Strength Unitmg/1
Pharmacy ClassesProgesterone Congeners [CS],Progestin [EPC]

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