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Desonide
Desonide - 54868-5050-0 - (Desonide)
Drug Information of Desonide
| Product NDC: | 54868-5050 |
| Proprietary Name: | Desonide |
| 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 Desonide
| Product NDC: | 54868-5050 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA072354 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040517 |
Package Information of Desonide
| Package NDC: | 54868-5050-0 |
| Package Description: | 120 g in 1 BOTTLE, PLASTIC (54868-5050-0) |
NDC Information of Desonide
| NDC Code | 54868-5050-0 |
| Proprietary Name | Desonide |
| Package Description | 120 g in 1 BOTTLE, PLASTIC (54868-5050-0) |
| Product NDC | 54868-5050 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Desonide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20040517 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | DESONIDE |
| Strength Number | .5 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
