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hydrocortisone
hydrocortisone - 37808-885-64 - (Hydrocortisone)
Drug Information of hydrocortisone
| Product NDC: | 37808-885 |
| Proprietary Name: | hydrocortisone |
| Non Proprietary Name: | Hydrocortisone |
| Active Ingredient(s): | 1 g/100g & nbsp; Hydrocortisone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of hydrocortisone
| Product NDC: | 37808-885 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20101002 |
Package Information of hydrocortisone
| Package NDC: | 37808-885-64 |
| Package Description: | 1 TUBE in 1 CARTON (37808-885-64) > 28 g in 1 TUBE |
NDC Information of hydrocortisone
| NDC Code | 37808-885-64 |
| Proprietary Name | hydrocortisone |
| Package Description | 1 TUBE in 1 CARTON (37808-885-64) > 28 g in 1 TUBE |
| Product NDC | 37808-885 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Hydrocortisone |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20101002 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | H E B |
| Substance Name | HYDROCORTISONE |
| Strength Number | 1 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
