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Antipyrine and Benzocaine Otic - 42192-708-10 - (ANTIPYRINE, BENZOCAINE)

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Drug Information of Antipyrine and Benzocaine Otic

Product NDC: 42192-708
Proprietary Name: Antipyrine and Benzocaine Otic
Non Proprietary Name: ANTIPYRINE, BENZOCAINE
Active Ingredient(s): 54; 14    mg/mL; mg/mL & nbsp;   ANTIPYRINE, BENZOCAINE
Administration Route(s): AURICULAR (OTIC)
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Antipyrine and Benzocaine Otic

Product NDC: 42192-708
Labeler Name: Acella Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20101109

Package Information of Antipyrine and Benzocaine Otic

Package NDC: 42192-708-10
Package Description: 10 mL in 1 BOTTLE, DROPPER (42192-708-10)

NDC Information of Antipyrine and Benzocaine Otic

NDC Code 42192-708-10
Proprietary Name Antipyrine and Benzocaine Otic
Package Description 10 mL in 1 BOTTLE, DROPPER (42192-708-10)
Product NDC 42192-708
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ANTIPYRINE, BENZOCAINE
Dosage Form Name SOLUTION
Route Name AURICULAR (OTIC)
Start Marketing Date 20101109
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Acella Pharmaceuticals
Substance Name ANTIPYRINE; BENZOCAINE
Strength Number 54; 14
Strength Unit mg/mL; mg/mL
Pharmaceutical Classes Standardized Chemical Allergen [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient]

Complete Information of Antipyrine and Benzocaine Otic


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