"16571-116-50" National Drug Code (NDC)

NDC Code	16571-116-50
Package Description	500 TABLET in 1 BOTTLE (16571-116-50)
Product NDC	16571-116
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Gabapentin
Non-Proprietary Name	Gabapentin
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20230719
End Marketing Date	20260208
Marketing Category Name	ANDA
Application Number	ANDA217995
Manufacturer	Rising Pharma Holdings, Inc.
Substance Name	GABAPENTIN
Strength	600
Strength Unit	mg/1
Pharmacy Classes	Decreased Central Nervous System Disorganized Electrical Activity [PE]