"72789-323-21" National Drug Code (NDC)

Zolpidem Tartrate 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-323-21)
(PD-Rx Pharmaceuticals, Inc.)

NDC Code72789-323-21
Package Description21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-323-21)
Product NDC72789-323
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameZolpidem Tartrate
Non-Proprietary NameZolpidem Tartrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20070504
Marketing Category NameANDA
Application NumberANDA078413
ManufacturerPD-Rx Pharmaceuticals, 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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