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