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Benzonatate - 63629-2655-5 - (Benzonatate)

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Drug Information of Benzonatate

Product NDC: 63629-2655
Proprietary Name: Benzonatate
Non Proprietary Name: Benzonatate
Active Ingredient(s): 100    mg/1 & nbsp;   Benzonatate
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Benzonatate

Product NDC: 63629-2655
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA081297
Marketing Category: ANDA
Start Marketing Date: 19930401

Package Information of Benzonatate

Package NDC: 63629-2655-5
Package Description: 120 CAPSULE in 1 BOTTLE (63629-2655-5)

NDC Information of Benzonatate

NDC Code 63629-2655-5
Proprietary Name Benzonatate
Package Description 120 CAPSULE in 1 BOTTLE (63629-2655-5)
Product NDC 63629-2655
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Benzonatate
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19930401
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name BENZONATATE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Decreased Tracheobronchial Stretch Receptor Activity [PE],Non-narcotic Antitussive [EPC]

Complete Information of Benzonatate


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