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"68727-351-01" National Drug Code (NDC)

Sunosi 30 TABLET, FILM COATED in 1 BOTTLE (68727-351-01)
(Jazz Pharmaceuticals, Inc.)

NDC Code68727-351-01
Package Description30 TABLET, FILM COATED in 1 BOTTLE (68727-351-01)
Product NDC68727-351
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameSunosi
Non-Proprietary NameSolriamfetol
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190618
End Marketing Date20240331
Marketing Category NameNDA
Application NumberNDA211230
ManufacturerJazz Pharmaceuticals, Inc.
Substance NameSOLRIAMFETOL
Strength150
Strength Unitmg/1
Pharmacy ClassesDopamine Uptake Inhibitors [MoA], Dopamine and Norepinephrine Reuptake Inhibitor [EPC], Norepinephrine Uptake Inhibitors [MoA]
DEA ScheduleCIV

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