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HYDROCORTISONE
HYDROCORTISONE - 0168-0016-31 - (HYDROCORTISONE)
Drug Information of HYDROCORTISONE
| Product NDC: | 0168-0016 |
| Proprietary Name: | HYDROCORTISONE |
| Non Proprietary Name: | HYDROCORTISONE |
| Active Ingredient(s): | 5 mg/g & nbsp; HYDROCORTISONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of HYDROCORTISONE
| Product NDC: | 0168-0016 |
| Labeler Name: | E. Fougera & Co. a division of Fougera Pharmaceuticals Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19810101 |
Package Information of HYDROCORTISONE
| Package NDC: | 0168-0016-31 |
| Package Description: | 1 TUBE in 1 CARTON (0168-0016-31) > 28 g in 1 TUBE |
NDC Information of HYDROCORTISONE
| NDC Code | 0168-0016-31 |
| Proprietary Name | HYDROCORTISONE |
| Package Description | 1 TUBE in 1 CARTON (0168-0016-31) > 28 g in 1 TUBE |
| Product NDC | 0168-0016 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | HYDROCORTISONE |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 19810101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | E. Fougera & Co. a division of Fougera Pharmaceuticals Inc. |
| Substance Name | HYDROCORTISONE |
| Strength Number | 5 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
