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Hydrocortisone
Hydrocortisone - 50607-5802-1 - (Hydrocortisone)
Drug Information of Hydrocortisone
| Product NDC: | 50607-5802 |
| Proprietary Name: | Hydrocortisone |
| Non Proprietary Name: | Hydrocortisone |
| Active Ingredient(s): | 10 mg/g & nbsp; Hydrocortisone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydrocortisone
| Product NDC: | 50607-5802 |
| Labeler Name: | B8 Sales, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100501 |
Package Information of Hydrocortisone
| Package NDC: | 50607-5802-1 |
| Package Description: | 25 POUCH in 1 BOX (50607-5802-1) > .9 g in 1 POUCH |
NDC Information of Hydrocortisone
| NDC Code | 50607-5802-1 |
| Proprietary Name | Hydrocortisone |
| Package Description | 25 POUCH in 1 BOX (50607-5802-1) > .9 g in 1 POUCH |
| Product NDC | 50607-5802 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Hydrocortisone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100501 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | B8 Sales, Inc. |
| Substance Name | HYDROCORTISONE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
