"16714-891-01" National Drug Code (NDC)

NDC Code	16714-891-01
Package Description	9 TABLET, FILM COATED in 1 BOTTLE (16714-891-01)
Product NDC	16714-891
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Sumatriptan And Naproxen Sodium
Non-Proprietary Name	Sumatriptan And Naproxen Sodium
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20181127
Marketing Category Name	ANDA
Application Number	ANDA202803
Manufacturer	NorthStar RxLLC
Substance Name	NAPROXEN SODIUM; SUMATRIPTAN SUCCINATE
Strength	500; 85
Strength Unit	mg/1; mg/1
Pharmacy Classes	Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC], Serotonin 1b Receptor Agonists [MoA], Serotonin 1d Receptor Agonists [MoA], Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]