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Hydrocortisone Butyrate
Hydrocortisone Butyrate - 51672-4061-2 - (Hydrocortisone Butyrate)
Drug Information of Hydrocortisone Butyrate
| Product NDC: | 51672-4061 |
| Proprietary Name: | Hydrocortisone Butyrate |
| Non Proprietary Name: | Hydrocortisone Butyrate |
| Active Ingredient(s): | 1 mg/mL & nbsp; Hydrocortisone Butyrate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydrocortisone Butyrate
| Product NDC: | 51672-4061 |
| Labeler Name: | Taro Pharmaceuticals U.S.A., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076364 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040114 |
Package Information of Hydrocortisone Butyrate
| Package NDC: | 51672-4061-2 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (51672-4061-2) > 20 mL in 1 BOTTLE, PLASTIC |
NDC Information of Hydrocortisone Butyrate
| NDC Code | 51672-4061-2 |
| Proprietary Name | Hydrocortisone Butyrate |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (51672-4061-2) > 20 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 51672-4061 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocortisone Butyrate |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20040114 |
| Marketing Category Name | ANDA |
| Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
| Substance Name | HYDROCORTISONE BUTYRATE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
