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Pramosone
Pramosone - 0496-0726-06 - (hydrocortisone acetate and pramoxine hydrochloride)
Drug Information of Pramosone
| Product NDC: | 0496-0726 |
| Proprietary Name: | Pramosone |
| Non Proprietary Name: | hydrocortisone acetate and pramoxine hydrochloride |
| Active Ingredient(s): | 25; 10 mg/mL; mg/mL & nbsp; hydrocortisone acetate and pramoxine hydrochloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pramosone
| Product NDC: | 0496-0726 |
| Labeler Name: | Ferndale Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA085979 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19770730 |
Package Information of Pramosone
| Package NDC: | 0496-0726-06 |
| Package Description: | 59 mL in 1 BOTTLE, PLASTIC (0496-0726-06) |
NDC Information of Pramosone
| NDC Code | 0496-0726-06 |
| Proprietary Name | Pramosone |
| Package Description | 59 mL in 1 BOTTLE, PLASTIC (0496-0726-06) |
| Product NDC | 0496-0726 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | hydrocortisone acetate and pramoxine hydrochloride |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 19770730 |
| Marketing Category Name | ANDA |
| Labeler Name | Ferndale Laboratories, Inc. |
| Substance Name | HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE |
| Strength Number | 25; 10 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
