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Desonide
Desonide - 51672-1281-1 - (Desonide)
Drug Information of Desonide
| Product NDC: | 51672-1281 |
| 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: | 51672-1281 |
| Labeler Name: | Taro Pharmaceuticals U.S.A., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074254 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19940803 |
Package Information of Desonide
| Package NDC: | 51672-1281-1 |
| Package Description: | 1 TUBE in 1 CARTON (51672-1281-1) > 15 g in 1 TUBE |
NDC Information of Desonide
| NDC Code | 51672-1281-1 |
| Proprietary Name | Desonide |
| Package Description | 1 TUBE in 1 CARTON (51672-1281-1) > 15 g in 1 TUBE |
| Product NDC | 51672-1281 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Desonide |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 19940803 |
| Marketing Category Name | ANDA |
| Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
| Substance Name | DESONIDE |
| Strength Number | .5 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
