"71335-2186-1" National Drug Code (NDC)

Ramelteon 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2186-1)
(Bryant Ranch Prepack)

NDC Code71335-2186-1
Package Description30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2186-1)
Product NDC71335-2186
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRamelteon
Non-Proprietary NameRamelteon
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200630
Marketing Category NameANDA
Application NumberANDA212650
ManufacturerBryant Ranch Prepack
Substance NameRAMELTEON
Strength8
Strength Unitmg/1
Pharmacy ClassesMelatonin Receptor Agonist [EPC], Melatonin Receptor Agonists [MoA]

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