"80725-012-30" National Drug Code (NDC)

Lunesta 30 TABLET, COATED in 1 BOTTLE (80725-012-30)
(Waylis Therapeutics LLC)

NDC Code80725-012-30
Package Description30 TABLET, COATED in 1 BOTTLE (80725-012-30)
Product NDC80725-012
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLunesta
Non-Proprietary NameEszopiclone
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20230815
Marketing Category NameNDA
Application NumberNDA021476
ManufacturerWaylis Therapeutics LLC
Substance NameESZOPICLONE
Strength3
Strength Unitmg/1
DEA ScheduleCIV

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