"69539-016-90" National Drug Code (NDC)

NDC Code	69539-016-90
Package Description	90 CAPSULE in 1 BOTTLE (69539-016-90)
Product NDC	69539-016
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	MSN LABORATORIES PRIVATE LIMITED
Substance Name	PREGABALIN
Strength	200
Strength Unit	mg/1
DEA Schedule	CV