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PRAMCORT
PRAMCORT - 49908-150-30 - (1% HYDROCORTISONE ACETATE W/W 1% PRAMOXINE HYDROCHLORIDE W/W CREAM)
Drug Information of PRAMCORT
| Product NDC: | 49908-150 |
| Proprietary Name: | PRAMCORT |
| Non Proprietary Name: | 1% HYDROCORTISONE ACETATE W/W 1% PRAMOXINE HYDROCHLORIDE W/W CREAM |
| Active Ingredient(s): | 10; 10 mg/g; mg/g & nbsp; 1% HYDROCORTISONE ACETATE W/W 1% PRAMOXINE HYDROCHLORIDE W/W CREAM |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PRAMCORT
| Product NDC: | 49908-150 |
| Labeler Name: | Rochester Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110330 |
Package Information of PRAMCORT
| Package NDC: | 49908-150-30 |
| Package Description: | 1 TUBE, WITH APPLICATOR in 1 CARTON (49908-150-30) > 30 g in 1 TUBE, WITH APPLICATOR |
NDC Information of PRAMCORT
| NDC Code | 49908-150-30 |
| Proprietary Name | PRAMCORT |
| Package Description | 1 TUBE, WITH APPLICATOR in 1 CARTON (49908-150-30) > 30 g in 1 TUBE, WITH APPLICATOR |
| Product NDC | 49908-150 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | 1% HYDROCORTISONE ACETATE W/W 1% PRAMOXINE HYDROCHLORIDE W/W CREAM |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110330 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Rochester Pharmaceuticals |
| 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] |
