"72789-127-90" National Drug Code (NDC)

NDC Code	72789-127-90
Package Description	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-127-90)
Product NDC	72789-127
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Gabapentin
Non-Proprietary Name	Gabapentin
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20121016
Marketing Category Name	ANDA
Application Number	ANDA078926
Manufacturer	PD-Rx Pharmaceuticals, Inc.
Substance Name	GABAPENTIN
Strength	600
Strength Unit	mg/1
Pharmacy Classes	Decreased Central Nervous System Disorganized Electrical Activity [PE]