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hydrocortisone
hydrocortisone - 54569-1118-0 - (hydrocortisone)
Drug Information of hydrocortisone
| Product NDC: | 54569-1118 |
| Proprietary Name: | hydrocortisone |
| Non Proprietary Name: | hydrocortisone |
| Active Ingredient(s): | 1 g/100g & nbsp; hydrocortisone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of hydrocortisone
| Product NDC: | 54569-1118 |
| Labeler Name: | A-S Medication Solutions LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110818 |
Package Information of hydrocortisone
| Package NDC: | 54569-1118-0 |
| Package Description: | 1 TUBE in 1 CARTON (54569-1118-0) > 30 g in 1 TUBE |
NDC Information of hydrocortisone
| NDC Code | 54569-1118-0 |
| Proprietary Name | hydrocortisone |
| Package Description | 1 TUBE in 1 CARTON (54569-1118-0) > 30 g in 1 TUBE |
| Product NDC | 54569-1118 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | hydrocortisone |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20110818 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | A-S Medication Solutions LLC |
| Substance Name | HYDROCORTISONE |
| Strength Number | 1 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
