"72189-153-30" National Drug Code (NDC)

Ramelteon 30 TABLET in 1 BOTTLE (72189-153-30)
(DIRECT RX)

NDC Code72189-153-30
Package Description30 TABLET in 1 BOTTLE (72189-153-30)
Product NDC72189-153
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRamelteon
Non-Proprietary NameRamelteon
Dosage FormTABLET
UsageORAL
Start Marketing Date20201103
Marketing Category NameANDA
Application NumberANDA211567
ManufacturerDIRECT RX
Substance NameRAMELTEON
Strength8
Strength Unitmg/1
Pharmacy ClassesMelatonin Receptor Agonist [EPC], Melatonin Receptor Agonists [MoA]

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