"17856-0600-1" National Drug Code (NDC)

NDC Code	17856-0600-1
Package Description	72 CUP, UNIT-DOSE in 1 BOX (17856-0600-1) / 5 mL in 1 CUP, UNIT-DOSE (17856-0600-4)
Product NDC	17856-0600
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Gabapentin
Non-Proprietary Name	Gabapentin
Dosage Form	SOLUTION
Usage	ORAL
Start Marketing Date	20180629
Marketing Category Name	ANDA
Application Number	ANDA076403
Manufacturer	ATLANTIC BIOLOGICALS CORP.
Substance Name	GABAPENTIN
Strength	250
Strength Unit	mg/5mL
Pharmacy Classes	Decreased Central Nervous System Disorganized Electrical Activity [PE]