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Cormax
Cormax - 52544-048-86 - (clobetasol propionate)
Drug Information of Cormax
| Product NDC: | 52544-048 |
| Proprietary Name: | Cormax |
| Non Proprietary Name: | clobetasol propionate |
| Active Ingredient(s): | .5 mg/g & nbsp; clobetasol propionate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cormax
| Product NDC: | 52544-048 |
| Labeler Name: | Watson Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074221 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080918 |
Package Information of Cormax
| Package NDC: | 52544-048-86 |
| Package Description: | 1 TUBE in 1 CARTON (52544-048-86) > 15 g in 1 TUBE |
NDC Information of Cormax
| NDC Code | 52544-048-86 |
| Proprietary Name | Cormax |
| Package Description | 1 TUBE in 1 CARTON (52544-048-86) > 15 g in 1 TUBE |
| Product NDC | 52544-048 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | clobetasol propionate |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20080918 |
| Marketing Category Name | ANDA |
| Labeler Name | Watson Pharma, Inc. |
| Substance Name | CLOBETASOL PROPIONATE |
| Strength Number | .5 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
