"51224-001-50" National Drug Code (NDC)

NDC Code	51224-001-50
Package Description	100 CAPSULE in 1 BOTTLE (51224-001-50)
Product NDC	51224-001
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Benzonatate
Non-Proprietary Name	Benzonatate
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20150810
Marketing Category Name	ANDA
Application Number	ANDA202765
Manufacturer	TAGI Pharma, Inc.
Substance Name	BENZONATATE
Strength	200
Strength Unit	mg/1
Pharmacy Classes	Decreased Tracheobronchial Stretch Receptor Activity [PE], Non-narcotic Antitussive [EPC]