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Benzonatate - 55154-2063-0 - (Benzonatate)

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Drug Information of Benzonatate

Product NDC: 55154-2063
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: 55154-2063
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040597
Marketing Category: ANDA
Start Marketing Date: 20070904

Package Information of Benzonatate

Package NDC: 55154-2063-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-2063-0) > 1 CAPSULE in 1 BLISTER PACK

NDC Information of Benzonatate

NDC Code 55154-2063-0
Proprietary Name Benzonatate
Package Description 10 BLISTER PACK in 1 BAG (55154-2063-0) > 1 CAPSULE in 1 BLISTER PACK
Product NDC 55154-2063
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Benzonatate
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20070904
Marketing Category Name ANDA
Labeler Name Cardinal Health
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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