"50111-851-01" National Drug Code (NDC)

NDC Code	50111-851-01
Package Description	100 CAPSULE in 1 BOTTLE (50111-851-01)
Product NDC	50111-851
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Benzonatate
Non-Proprietary Name	Benzonatate
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	19930401
End Marketing Date	20150831
Marketing Category Name	ANDA
Application Number	ANDA081297
Manufacturer	Pliva Inc.
Substance Name	BENZONATATE
Strength	100
Strength Unit	mg/1
Pharmacy Classes	Decreased Tracheobronchial Stretch Receptor Activity [PE],Non-narcotic Antitussive [EPC]