"72205-016-06" National Drug Code (NDC)

NDC Code	72205-016-06
Package Description	100 BLISTER PACK in 1 CARTON (72205-016-06) / 10 CAPSULE in 1 BLISTER PACK (72205-016-11)
Product NDC	72205-016
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Pregabalin
Non-Proprietary Name	Pregabalin
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20190719
Marketing Category Name	ANDA
Application Number	ANDA209357
Manufacturer	Novadoz Pharmaceuticals LLC
Substance Name	PREGABALIN
Strength	200
Strength Unit	mg/1
DEA Schedule	CV