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desonide
desonide - 0168-0309-15 - (desonide)
Drug Information of desonide
| Product NDC: | 0168-0309 |
| Proprietary Name: | desonide |
| Non Proprietary Name: | desonide |
| Active Ingredient(s): | .5 mg/g & nbsp; desonide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of desonide
| Product NDC: | 0168-0309 |
| Labeler Name: | E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075751 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101019 |
Package Information of desonide
| Package NDC: | 0168-0309-15 |
| Package Description: | 1 TUBE in 1 CARTON (0168-0309-15) > 15 g in 1 TUBE |
NDC Information of desonide
| NDC Code | 0168-0309-15 |
| Proprietary Name | desonide |
| Package Description | 1 TUBE in 1 CARTON (0168-0309-15) > 15 g in 1 TUBE |
| Product NDC | 0168-0309 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | desonide |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20101019 |
| Marketing Category Name | ANDA |
| Labeler Name | E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc. |
| Substance Name | DESONIDE |
| Strength Number | .5 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
