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Clobetasol Propionate
Clobetasol Propionate - 60432-133-50 - (CLOBETASOL PROPIONATE)
Drug Information of Clobetasol Propionate
| Product NDC: | 60432-133 |
| Proprietary Name: | Clobetasol Propionate |
| Non Proprietary Name: | CLOBETASOL PROPIONATE |
| Active Ingredient(s): | .5 mg/mL & nbsp; CLOBETASOL PROPIONATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Clobetasol Propionate
| Product NDC: | 60432-133 |
| Labeler Name: | Morton Grove Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075205 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19981113 |
Package Information of Clobetasol Propionate
| Package NDC: | 60432-133-50 |
| Package Description: | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (60432-133-50) > 50 mL in 1 BOTTLE, WITH APPLICATOR |
NDC Information of Clobetasol Propionate
| NDC Code | 60432-133-50 |
| Proprietary Name | Clobetasol Propionate |
| Package Description | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (60432-133-50) > 50 mL in 1 BOTTLE, WITH APPLICATOR |
| Product NDC | 60432-133 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CLOBETASOL PROPIONATE |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 19981113 |
| Marketing Category Name | ANDA |
| Labeler Name | Morton Grove Pharmaceuticals, Inc. |
| Substance Name | CLOBETASOL PROPIONATE |
| Strength Number | .5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
