"70518-1663-1" National Drug Code (NDC)

Zolpidem Tartrate 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1663-1)
(REMEDYREPACK INC.)

NDC Code70518-1663-1
Package Description30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1663-1)
Product NDC70518-1663
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameZolpidem Tartrate
Non-Proprietary NameZolpidem Tartrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20181112
Marketing Category NameANDA
Application NumberANDA076410
ManufacturerREMEDYREPACK INC.
Substance NameZOLPIDEM TARTRATE
Strength10
Strength Unitmg/1
Pharmacy ClassesCentral Nervous System Depression [PE], GABA A Receptor Positive Modulators [MoA], gamma-Aminobutyric Acid A Receptor Positive Modulator [EPC]
DEA ScheduleCIV

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