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benzonatate - 21695-191-15 - (benzonatate)

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Drug Information of benzonatate

Product NDC: 21695-191
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: 21695-191
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040627
Marketing Category: ANDA
Start Marketing Date: 20070725

Package Information of benzonatate

Package NDC: 21695-191-15
Package Description: 15 CAPSULE in 1 BOTTLE (21695-191-15)

NDC Information of benzonatate

NDC Code 21695-191-15
Proprietary Name benzonatate
Package Description 15 CAPSULE in 1 BOTTLE (21695-191-15)
Product NDC 21695-191
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 Rebel Distributors Corp
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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