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Oto End 10
Oto End 10 - 68047-051-10 - (Pramoxine HCl / Hydrocortisone / Chloroxylenol)
Drug Information of Oto End 10
| Product NDC: | 68047-051 |
| Proprietary Name: | Oto End 10 |
| Non Proprietary Name: | Pramoxine HCl / Hydrocortisone / Chloroxylenol |
| Active Ingredient(s): | 1; 10; 10 mg/mL; mg/mL; mg/mL & nbsp; Pramoxine HCl / Hydrocortisone / Chloroxylenol |
| Administration Route(s): | AURICULAR (OTIC) |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Oto End 10
| Product NDC: | 68047-051 |
| Labeler Name: | Larken Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20071012 |
Package Information of Oto End 10
| Package NDC: | 68047-051-10 |
| Package Description: | 1 BOTTLE, DROPPER in 1 PACKAGE (68047-051-10) > 10 mL in 1 BOTTLE, DROPPER |
NDC Information of Oto End 10
| NDC Code | 68047-051-10 |
| Proprietary Name | Oto End 10 |
| Package Description | 1 BOTTLE, DROPPER in 1 PACKAGE (68047-051-10) > 10 mL in 1 BOTTLE, DROPPER |
| Product NDC | 68047-051 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Pramoxine HCl / Hydrocortisone / Chloroxylenol |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | AURICULAR (OTIC) |
| Start Marketing Date | 20071012 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Larken Laboratories, Inc. |
| Substance Name | CHLOROXYLENOL; HYDROCORTISONE; PRAMOXINE HYDROCHLORIDE |
| Strength Number | 1; 10; 10 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
