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Analpram E
Analpram E - 0496-0755-64 - (hydrocortisone acetate and pramoxine hydrochloride)
Drug Information of Analpram E
| Product NDC: | 0496-0755 |
| Proprietary Name: | Analpram E |
| Non Proprietary Name: | hydrocortisone acetate and pramoxine hydrochloride |
| Active Ingredient(s): | 25; 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 Analpram E
| Product NDC: | 0496-0755 |
| Labeler Name: | Ferndale Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20090630 |
Package Information of Analpram E
| Package NDC: | 0496-0755-64 |
| Package Description: | 30 TUBE, WITH APPLICATOR in 1 CARTON (0496-0755-64) > 4 g in 1 TUBE, WITH APPLICATOR (0496-0755-36) |
NDC Information of Analpram E
| NDC Code | 0496-0755-64 |
| Proprietary Name | Analpram E |
| Package Description | 30 TUBE, WITH APPLICATOR in 1 CARTON (0496-0755-64) > 4 g in 1 TUBE, WITH APPLICATOR (0496-0755-36) |
| Product NDC | 0496-0755 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | hydrocortisone acetate and pramoxine hydrochloride |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20090630 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Ferndale Laboratories, Inc. |
| Substance Name | HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE |
| Strength Number | 25; 10 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
