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Hydrocortisone
Hydrocortisone - 0168-0288-02 - (hydrocortisone)
Drug Information of Hydrocortisone
| Product NDC: | 0168-0288 |
| Proprietary Name: | Hydrocortisone |
| Non Proprietary Name: | hydrocortisone |
| Active Ingredient(s): | 25 mg/mL & nbsp; hydrocortisone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydrocortisone
| Product NDC: | 0168-0288 |
| Labeler Name: | E.FOUGERA & COMPANY A division of Fougera Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040351 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20000725 |
Package Information of Hydrocortisone
| Package NDC: | 0168-0288-02 |
| Package Description: | 59 mL in 1 BOTTLE (0168-0288-02) |
NDC Information of Hydrocortisone
| NDC Code | 0168-0288-02 |
| Proprietary Name | Hydrocortisone |
| Package Description | 59 mL in 1 BOTTLE (0168-0288-02) |
| Product NDC | 0168-0288 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | hydrocortisone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20000725 |
| Marketing Category Name | ANDA |
| Labeler Name | E.FOUGERA & COMPANY A division of Fougera Pharmaceuticals Inc. |
| Substance Name | HYDROCORTISONE |
| Strength Number | 25 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
