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DesOwen
DesOwen - 0299-5765-04 - (desonide)
Drug Information of DesOwen
| Product NDC: | 0299-5765 |
| Proprietary Name: | DesOwen |
| Non Proprietary Name: | desonide |
| Active Ingredient(s): | .5 mg/g & nbsp; desonide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DesOwen
| Product NDC: | 0299-5765 |
| Labeler Name: | Galderma Laboratories, L.P. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA072354 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19880715 |
Package Information of DesOwen
| Package NDC: | 0299-5765-04 |
| Package Description: | 118 g in 1 BOTTLE (0299-5765-04) |
NDC Information of DesOwen
| NDC Code | 0299-5765-04 |
| Proprietary Name | DesOwen |
| Package Description | 118 g in 1 BOTTLE (0299-5765-04) |
| Product NDC | 0299-5765 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | desonide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 19880715 |
| Marketing Category Name | ANDA |
| Labeler Name | Galderma Laboratories, L.P. |
| Substance Name | DESONIDE |
| Strength Number | .5 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
