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benzonatate - 55289-996-30 - (benzonatate)

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Drug Information of benzonatate

Product NDC: 55289-996
Proprietary Name: benzonatate
Non Proprietary Name: benzonatate
Active Ingredient(s): 200    mg/1 & nbsp;   benzonatate
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of benzonatate

Product NDC: 55289-996
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040749
Marketing Category: ANDA
Start Marketing Date: 20070725

Package Information of benzonatate

Package NDC: 55289-996-30
Package Description: 30 CAPSULE in 1 BOTTLE, PLASTIC (55289-996-30)

NDC Information of benzonatate

NDC Code 55289-996-30
Proprietary Name benzonatate
Package Description 30 CAPSULE in 1 BOTTLE, PLASTIC (55289-996-30)
Product NDC 55289-996
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 PD-Rx Pharmaceuticals, Inc.
Substance Name BENZONATATE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Decreased Tracheobronchial Stretch Receptor Activity [PE],Non-narcotic Antitussive [EPC]

Complete Information of benzonatate


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