"70934-002-30" National Drug Code (NDC)

NDC Code	70934-002-30
Package Description	30 TABLET in 1 BOTTLE, PLASTIC (70934-002-30)
Product NDC	70934-002
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Aripiprazole
Non-Proprietary Name	Aripiprazole
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20170221
Marketing Category Name	ANDA
Application Number	ANDA201519
Manufacturer	Denton Pharma, Inc. DBA Northwind Pharmaceuticals
Substance Name	ARIPIPRAZOLE
Strength	5
Strength Unit	mg/1
Pharmacy Classes	Atypical Antipsychotic [EPC]