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ZyPram
ZyPram - 68025-040-30 - (Hydrocortisone Acetate and Pramoxine Hydrochloride)
Drug Information of ZyPram
| Product NDC: | 68025-040 |
| Proprietary Name: | ZyPram |
| Non Proprietary Name: | Hydrocortisone Acetate and Pramoxine Hydrochloride |
| Active Ingredient(s): | 705; 300 mg/30g; mg/30g & nbsp; Hydrocortisone Acetate and Pramoxine Hydrochloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ZyPram
| Product NDC: | 68025-040 |
| Labeler Name: | Vertical Pharmaceuticals, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED OTHER |
| Start Marketing Date: | 20090721 |
Package Information of ZyPram
| Package NDC: | 68025-040-30 |
| Package Description: | 30 g in 1 TUBE (68025-040-30) |
NDC Information of ZyPram
| NDC Code | 68025-040-30 |
| Proprietary Name | ZyPram |
| Package Description | 30 g in 1 TUBE (68025-040-30) |
| Product NDC | 68025-040 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocortisone Acetate and Pramoxine Hydrochloride |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20090721 |
| Marketing Category Name | UNAPPROVED OTHER |
| Labeler Name | Vertical Pharmaceuticals, Inc |
| Substance Name | HYDROCORTISONE ACETATE; PRAMOXINE HYDROCHLORIDE |
| Strength Number | 705; 300 |
| Strength Unit | mg/30g; mg/30g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
