Tessalon - 0069-0124-01 - (benzonatate)

Alphabetical Index


Drug Information of Tessalon

Product NDC: 0069-0124
Proprietary Name: Tessalon
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 Tessalon

Product NDC: 0069-0124
Labeler Name: Pfizer Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA011210
Marketing Category: NDA
Start Marketing Date: 19990625

Package Information of Tessalon

Package NDC: 0069-0124-01
Package Description: 100 CAPSULE in 1 BOTTLE (0069-0124-01)

NDC Information of Tessalon

NDC Code 0069-0124-01
Proprietary Name Tessalon
Package Description 100 CAPSULE in 1 BOTTLE (0069-0124-01)
Product NDC 0069-0124
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name benzonatate
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19990625
Marketing Category Name NDA
Labeler Name Pfizer Laboratories
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 Tessalon


General Information