"47335-978-13" National Drug Code (NDC)

NDC Code	47335-978-13
Package Description	500 TABLET, FILM COATED in 1 BOTTLE (47335-978-13)
Product NDC	47335-978
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Zolmitriptan
Non-Proprietary Name	Zolmitriptan
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20141124
Marketing Category Name	ANDA
Application Number	ANDA203476
Manufacturer	Sun Pharma Global FZE
Substance Name	ZOLMITRIPTAN
Strength	2.5
Strength Unit	mg/1
Pharmacy Classes	Serotonin 1b Receptor Agonists [MoA],Serotonin 1d Receptor Agonists [MoA],Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]