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Proctofoam
Proctofoam - 21695-982-10 - (hydrocortisone acetate and pramoxine hydrochloride)
Drug Information of Proctofoam
| Product NDC: | 21695-982 |
| Proprietary Name: | Proctofoam |
| Non Proprietary Name: | hydrocortisone acetate and pramoxine hydrochloride |
| Active Ingredient(s): | 100; 100 mg/10g; mg/10g & nbsp; hydrocortisone acetate and pramoxine hydrochloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | AEROSOL, FOAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Proctofoam
| Product NDC: | 21695-982 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA086195 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19780726 |
Package Information of Proctofoam
| Package NDC: | 21695-982-10 |
| Package Description: | 1 CONTAINER in 1 CARTON (21695-982-10) > 10 g in 1 CONTAINER |
NDC Information of Proctofoam
| NDC Code | 21695-982-10 |
| Proprietary Name | Proctofoam |
| Package Description | 1 CONTAINER in 1 CARTON (21695-982-10) > 10 g in 1 CONTAINER |
| Product NDC | 21695-982 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | hydrocortisone acetate and pramoxine hydrochloride |
| Dosage Form Name | AEROSOL, FOAM |
| Route Name | TOPICAL |
| Start Marketing Date | 19780726 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE |
| Strength Number | 100; 100 |
| Strength Unit | mg/10g; mg/10g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
