"60687-838-01" National Drug Code (NDC)

Zolpidem Tartrate 100 BLISTER PACK in 1 CARTON (60687-838-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-838-11)
(American Health Packaging)

NDC Code60687-838-01
Package Description100 BLISTER PACK in 1 CARTON (60687-838-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-838-11)
Product NDC60687-838
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameZolpidem Tartrate
Non-Proprietary NameZolpidem Tartrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20240901
Marketing Category NameANDA
Application NumberANDA078413
ManufacturerAmerican Health Packaging
Substance NameZOLPIDEM TARTRATE
Strength5
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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