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Hydrocortisone Acetate and Pramoxine Hydrochloride
Hydrocortisone Acetate and Pramoxine Hydrochloride - 42192-109-01 - (Hydrocortisone Acetate and Pramoxine Hydrochloride)
Drug Information of Hydrocortisone Acetate and Pramoxine Hydrochloride
| Product NDC: | 42192-109 |
| Proprietary Name: | Hydrocortisone Acetate and Pramoxine Hydrochloride |
| Non Proprietary Name: | Hydrocortisone Acetate and Pramoxine Hydrochloride |
| Active Ingredient(s): | 10; 10 mg/g; mg/g & nbsp; Hydrocortisone Acetate and Pramoxine Hydrochloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydrocortisone Acetate and Pramoxine Hydrochloride
| Product NDC: | 42192-109 |
| Labeler Name: | Acella Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20081103 |
Package Information of Hydrocortisone Acetate and Pramoxine Hydrochloride
| Package NDC: | 42192-109-01 |
| Package Description: | 28 g in 1 TUBE (42192-109-01) |
NDC Information of Hydrocortisone Acetate and Pramoxine Hydrochloride
| NDC Code | 42192-109-01 |
| Proprietary Name | Hydrocortisone Acetate and Pramoxine Hydrochloride |
| Package Description | 28 g in 1 TUBE (42192-109-01) |
| Product NDC | 42192-109 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocortisone Acetate and Pramoxine Hydrochloride |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20081103 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Acella Pharmaceuticals, LLC |
| Substance Name | HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE |
| Strength Number | 10; 10 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
