"57237-012-06" National Drug Code (NDC)

NDC Code	57237-012-06
Package Description	5 BLISTER PACK in 1 CARTON (57237-012-06) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Product NDC	57237-012
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Mirtazapine
Non-Proprietary Name	Mirtazapine
Dosage Form	TABLET, ORALLY DISINTEGRATING
Usage	ORAL
Start Marketing Date	20051208
Marketing Category Name	ANDA
Application Number	ANDA077376
Manufacturer	Rising Pharma Holdings, Inc.
Substance Name	MIRTAZAPINE
Strength	30
Strength Unit	mg/1