Home > National Drug Code (NDC) > benzonatate

benzonatate - 63629-4126-4 - (benzonatate)

Alphabetical Index


Drug Information of benzonatate

Product NDC: 63629-4126
Proprietary Name: benzonatate
Non Proprietary Name: benzonatate
Active Ingredient(s): 200    mg/1 & nbsp;   benzonatate
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of benzonatate

Product NDC: 63629-4126
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040749
Marketing Category: ANDA
Start Marketing Date: 20070725

Package Information of benzonatate

Package NDC: 63629-4126-4
Package Description: 20 CAPSULE in 1 BOTTLE (63629-4126-4)

NDC Information of benzonatate

NDC Code 63629-4126-4
Proprietary Name benzonatate
Package Description 20 CAPSULE in 1 BOTTLE (63629-4126-4)
Product NDC 63629-4126
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name benzonatate
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20070725
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name BENZONATATE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Decreased Tracheobronchial Stretch Receptor Activity [PE],Non-narcotic Antitussive [EPC]

Complete Information of benzonatate


General Information