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Hydrocortisone Valerate
Hydrocortisone Valerate - 51672-1290-1 - (Hydrocortisone Valerate)
Drug Information of Hydrocortisone Valerate
| Product NDC: | 51672-1290 |
| Proprietary Name: | Hydrocortisone Valerate |
| Non Proprietary Name: | Hydrocortisone Valerate |
| Active Ingredient(s): | 2 mg/g & nbsp; Hydrocortisone Valerate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydrocortisone Valerate
| Product NDC: | 51672-1290 |
| Labeler Name: | Taro Pharmaceuticals U.S.A., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075042 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19980825 |
Package Information of Hydrocortisone Valerate
| Package NDC: | 51672-1290-1 |
| Package Description: | 1 TUBE in 1 CARTON (51672-1290-1) > 15 g in 1 TUBE |
NDC Information of Hydrocortisone Valerate
| NDC Code | 51672-1290-1 |
| Proprietary Name | Hydrocortisone Valerate |
| Package Description | 1 TUBE in 1 CARTON (51672-1290-1) > 15 g in 1 TUBE |
| Product NDC | 51672-1290 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocortisone Valerate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 19980825 |
| Marketing Category Name | ANDA |
| Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
| Substance Name | HYDROCORTISONE VALERATE |
| Strength Number | 2 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
