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Hydrocortisone
Hydrocortisone - 49314-5801-0 - (Hydrocortisone)
Drug Information of Hydrocortisone
| Product NDC: | 49314-5801 |
| Proprietary Name: | Hydrocortisone |
| Non Proprietary Name: | Hydrocortisone |
| Active Ingredient(s): | 10 mg/mL & nbsp; Hydrocortisone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydrocortisone
| Product NDC: | 49314-5801 |
| Labeler Name: | UniShield |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100728 |
Package Information of Hydrocortisone
| Package NDC: | 49314-5801-0 |
| Package Description: | .8 mL in 1 PACKET (49314-5801-0) |
NDC Information of Hydrocortisone
| NDC Code | 49314-5801-0 |
| Proprietary Name | Hydrocortisone |
| Package Description | .8 mL in 1 PACKET (49314-5801-0) |
| Product NDC | 49314-5801 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Hydrocortisone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100728 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | UniShield |
| Substance Name | HYDROCORTISONE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
