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Benzonatate - 68788-9827-3 - (Benzonatate)

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Drug Information of Benzonatate

Product NDC: 68788-9827
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: 68788-9827
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040682
Marketing Category: ANDA
Start Marketing Date: 20120405

Package Information of Benzonatate

Package NDC: 68788-9827-3
Package Description: 30 CAPSULE, LIQUID FILLED in 1 BOTTLE (68788-9827-3)

NDC Information of Benzonatate

NDC Code 68788-9827-3
Proprietary Name Benzonatate
Package Description 30 CAPSULE, LIQUID FILLED in 1 BOTTLE (68788-9827-3)
Product NDC 68788-9827
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Benzonatate
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20120405
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, 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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