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Benzonatate - 68382-248-01 - (Benzonatate)

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Drug Information of Benzonatate

Product NDC: 68382-248
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: 68382-248
Labeler Name: Zydus Pharmaceuticals (USA) Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040597
Marketing Category: ANDA
Start Marketing Date: 20070904

Package Information of Benzonatate

Package NDC: 68382-248-01
Package Description: 100 CAPSULE in 1 BOTTLE (68382-248-01)

NDC Information of Benzonatate

NDC Code 68382-248-01
Proprietary Name Benzonatate
Package Description 100 CAPSULE in 1 BOTTLE (68382-248-01)
Product NDC 68382-248
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 Zydus Pharmaceuticals (USA) 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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