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Benzonatate - 67296-0567-1 - (Benzonatate)

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Drug Information of Benzonatate

Product NDC: 67296-0567
Proprietary Name: Benzonatate
Non Proprietary Name: Benzonatate
Active Ingredient(s): 100    mg/1 & nbsp;   Benzonatate
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Benzonatate

Product NDC: 67296-0567
Labeler Name: RedPharm Drug Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040682
Marketing Category: ANDA
Start Marketing Date: 20100113

Package Information of Benzonatate

Package NDC: 67296-0567-1
Package Description: 15 CAPSULE, LIQUID FILLED in 1 BOTTLE (67296-0567-1)

NDC Information of Benzonatate

NDC Code 67296-0567-1
Proprietary Name Benzonatate
Package Description 15 CAPSULE, LIQUID FILLED in 1 BOTTLE (67296-0567-1)
Product NDC 67296-0567
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Benzonatate
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20100113
Marketing Category Name ANDA
Labeler Name RedPharm Drug Inc.
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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