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Aurodex
Aurodex - 0904-6317-10 - (ANTIPYRINE, BENZOCAINE OTIC)
Drug Information of Aurodex
| Product NDC: | 0904-6317 |
| Proprietary Name: | Aurodex |
| Non Proprietary Name: | ANTIPYRINE, BENZOCAINE OTIC |
| Active Ingredient(s): | 54; 14 mg/mL; mg/mL & nbsp; ANTIPYRINE, BENZOCAINE OTIC |
| Administration Route(s): | AURICULAR (OTIC) |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aurodex
| Product NDC: | 0904-6317 |
| Labeler Name: | Major Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20090827 |
Package Information of Aurodex
| Package NDC: | 0904-6317-10 |
| Package Description: | 10 mL in 1 BOTTLE, DROPPER (0904-6317-10) |
NDC Information of Aurodex
| NDC Code | 0904-6317-10 |
| Proprietary Name | Aurodex |
| Package Description | 10 mL in 1 BOTTLE, DROPPER (0904-6317-10) |
| Product NDC | 0904-6317 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ANTIPYRINE, BENZOCAINE OTIC |
| Dosage Form Name | SOLUTION |
| Route Name | AURICULAR (OTIC) |
| Start Marketing Date | 20090827 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Major 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] |
