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DESONIDE
DESONIDE - 21695-944-15 - (DESONIDE)
Drug Information of DESONIDE
| Product NDC: | 21695-944 |
| Proprietary Name: | DESONIDE |
| Non Proprietary Name: | DESONIDE |
| Active Ingredient(s): | .5 mg/g & nbsp; DESONIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DESONIDE
| Product NDC: | 21695-944 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA073548 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19920630 |
Package Information of DESONIDE
| Package NDC: | 21695-944-15 |
| Package Description: | 1 TUBE in 1 CARTON (21695-944-15) > 15 g in 1 TUBE |
NDC Information of DESONIDE
| NDC Code | 21695-944-15 |
| Proprietary Name | DESONIDE |
| Package Description | 1 TUBE in 1 CARTON (21695-944-15) > 15 g in 1 TUBE |
| Product NDC | 21695-944 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DESONIDE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 19920630 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | DESONIDE |
| Strength Number | .5 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
