"0004-6202-01" National Drug Code (NDC)

NDC Code	0004-6202-01
Package Description	100 TABLET in 1 BOTTLE, PLASTIC (0004-6202-01)
Product NDC	0004-6202
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Anaprox
Non-Proprietary Name	Naproxen Sodium
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	19800904
End Marketing Date	20170131
Marketing Category Name	NDA
Application Number	NDA018164
Manufacturer	Genentech, Inc.
Substance Name	NAPROXEN SODIUM
Strength	275
Strength Unit	mg/1
Pharmacy Classes	Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]