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DESONATE
DESONATE - 10922-828-06 - (desonide)
Drug Information of DESONATE
| Product NDC: | 10922-828 |
| Proprietary Name: | DESONATE |
| Non Proprietary Name: | desonide |
| Active Ingredient(s): | .5 mg/g & nbsp; desonide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DESONATE
| Product NDC: | 10922-828 |
| Labeler Name: | Intendis Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021844 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100128 |
Package Information of DESONATE
| Package NDC: | 10922-828-06 |
| Package Description: | 1 TUBE in 1 CARTON (10922-828-06) > 60 g in 1 TUBE |
NDC Information of DESONATE
| NDC Code | 10922-828-06 |
| Proprietary Name | DESONATE |
| Package Description | 1 TUBE in 1 CARTON (10922-828-06) > 60 g in 1 TUBE |
| Product NDC | 10922-828 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | desonide |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20100128 |
| Marketing Category Name | NDA |
| Labeler Name | Intendis Inc. |
| Substance Name | DESONIDE |
| Strength Number | .5 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
