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Aurodex
Aurodex - 68788-0008-1 - (A/B Otic Drops)
Drug Information of Aurodex
| Product NDC: | 68788-0008 |
| Proprietary Name: | Aurodex |
| Non Proprietary Name: | A/B Otic Drops |
| Active Ingredient(s): | 54; 14 mg/mL; mg/mL & nbsp; A/B Otic Drops |
| Administration Route(s): | AURICULAR (OTIC) |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aurodex
| Product NDC: | 68788-0008 |
| Labeler Name: | Preferred Pharmaceuticals, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20101218 |
Package Information of Aurodex
| Package NDC: | 68788-0008-1 |
| Package Description: | 15 mL in 1 BOTTLE, DROPPER (68788-0008-1) |
NDC Information of Aurodex
| NDC Code | 68788-0008-1 |
| Proprietary Name | Aurodex |
| Package Description | 15 mL in 1 BOTTLE, DROPPER (68788-0008-1) |
| Product NDC | 68788-0008 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | A/B Otic Drops |
| Dosage Form Name | SOLUTION |
| Route Name | AURICULAR (OTIC) |
| Start Marketing Date | 20101218 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Preferred Pharmaceuticals, Inc |
| 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] |
