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Hydrocortisone
Hydrocortisone - 0472-0337-16 - (Hydrocortisone)
Drug Information of Hydrocortisone
| Product NDC: | 0472-0337 |
| Proprietary Name: | Hydrocortisone |
| Non Proprietary Name: | Hydrocortisone |
| Active Ingredient(s): | 25 mg/g & nbsp; Hydrocortisone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydrocortisone
| Product NDC: | 0472-0337 |
| Labeler Name: | Actavis Mid Atlantic LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089682 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20020930 |
Package Information of Hydrocortisone
| Package NDC: | 0472-0337-16 |
| Package Description: | 453.6 g in 1 JAR (0472-0337-16) |
NDC Information of Hydrocortisone
| NDC Code | 0472-0337-16 |
| Proprietary Name | Hydrocortisone |
| Package Description | 453.6 g in 1 JAR (0472-0337-16) |
| Product NDC | 0472-0337 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocortisone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20020930 |
| Marketing Category Name | ANDA |
| Labeler Name | Actavis Mid Atlantic LLC |
| Substance Name | HYDROCORTISONE |
| Strength Number | 25 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
