Zonatuss - 68025-058-10 - (benzonatate)

Alphabetical Index


Drug Information of Zonatuss

Product NDC: 68025-058
Proprietary Name: Zonatuss
Non Proprietary Name: benzonatate
Active Ingredient(s): 150    mg/1 & nbsp;   benzonatate
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Zonatuss

Product NDC: 68025-058
Labeler Name: Vertical Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040851
Marketing Category: ANDA
Start Marketing Date: 20111101

Package Information of Zonatuss

Package NDC: 68025-058-10
Package Description: 100 CAPSULE in 1 BOTTLE, PLASTIC (68025-058-10)

NDC Information of Zonatuss

NDC Code 68025-058-10
Proprietary Name Zonatuss
Package Description 100 CAPSULE in 1 BOTTLE, PLASTIC (68025-058-10)
Product NDC 68025-058
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name benzonatate
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20111101
Marketing Category Name ANDA
Labeler Name Vertical Pharmaceuticals, Inc.
Substance Name BENZONATATE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes Decreased Tracheobronchial Stretch Receptor Activity [PE],Non-narcotic Antitussive [EPC]

Complete Information of Zonatuss


General Information