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Acella Hydrocortisone Acetate - Pramoxine Singles
Acella Hydrocortisone Acetate - Pramoxine Singles - 42192-108-04 - (HYDROCORTISONE ACETATE, PRAMOXINE)
Drug Information of Acella Hydrocortisone Acetate - Pramoxine Singles
| Product NDC: | 42192-108 |
| Proprietary Name: | Acella Hydrocortisone Acetate - Pramoxine Singles |
| Non Proprietary Name: | HYDROCORTISONE ACETATE, PRAMOXINE |
| Active Ingredient(s): | 2.5; 1 g/100g; g/100g & nbsp; HYDROCORTISONE ACETATE, PRAMOXINE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Acella Hydrocortisone Acetate - Pramoxine Singles
| Product NDC: | 42192-108 |
| Labeler Name: | Acella Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20101108 |
Package Information of Acella Hydrocortisone Acetate - Pramoxine Singles
| Package NDC: | 42192-108-04 |
| Package Description: | 30 TUBE, WITH APPLICATOR in 1 CARTON (42192-108-04) > 4 g in 1 TUBE, WITH APPLICATOR |
NDC Information of Acella Hydrocortisone Acetate - Pramoxine Singles
| NDC Code | 42192-108-04 |
| Proprietary Name | Acella Hydrocortisone Acetate - Pramoxine Singles |
| Package Description | 30 TUBE, WITH APPLICATOR in 1 CARTON (42192-108-04) > 4 g in 1 TUBE, WITH APPLICATOR |
| Product NDC | 42192-108 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HYDROCORTISONE ACETATE, PRAMOXINE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20101108 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Acella Pharmaceuticals, LLC |
| Substance Name | HYDROCORTISONE ACETATE; PRAMOXINE |
| Strength Number | 2.5; 1 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
