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"61919-517-20" National Drug Code (NDC)
Benzonatate 20 CAPSULE in 1 BOTTLE (61919-517-20)
(Direct_Rx)
NDC Code
61919-517-20
Package Description
20 CAPSULE in 1 BOTTLE (61919-517-20)
Product NDC
61919-517
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Benzonatate
Non-Proprietary Name
Benzonatate
Dosage Form
CAPSULE
Usage
ORAL
Start Marketing Date
20190730
Marketing Category Name
ANDA
Application Number
ANDA040749
Manufacturer
Direct_Rx
Substance Name
BENZONATATE
Strength
200
Strength Unit
mg/1
Pharmacy Classes
Decreased Tracheobronchial Stretch Receptor Activity [PE], Non-narcotic Antitussive [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-517-20