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DESONIDE
DESONIDE - 0472-0803-02 - (DESONIDE LOTION 0.05%)
Drug Information of DESONIDE
| Product NDC: | 0472-0803 |
| Proprietary Name: | DESONIDE |
| Non Proprietary Name: | DESONIDE LOTION 0.05% |
| Active Ingredient(s): | .5 mg/g & nbsp; DESONIDE LOTION 0.05% |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DESONIDE
| Product NDC: | 0472-0803 |
| Labeler Name: | Actavis Mid Atlantic LLC, Lincolnton, NC 28092 |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA072354 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090528 |
Package Information of DESONIDE
| Package NDC: | 0472-0803-02 |
| Package Description: | 57.1 g in 1 BOTTLE, PLASTIC (0472-0803-02) |
NDC Information of DESONIDE
| NDC Code | 0472-0803-02 |
| Proprietary Name | DESONIDE |
| Package Description | 57.1 g in 1 BOTTLE, PLASTIC (0472-0803-02) |
| Product NDC | 0472-0803 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DESONIDE LOTION 0.05% |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20090528 |
| Marketing Category Name | ANDA |
| Labeler Name | Actavis Mid Atlantic LLC, Lincolnton, NC 28092 |
| Substance Name | DESONIDE |
| Strength Number | .5 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
