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Hydrocortisone
Hydrocortisone - 37808-929-64 - (Hydrocortisone Acetate)
Drug Information of Hydrocortisone
| Product NDC: | 37808-929 |
| Proprietary Name: | Hydrocortisone |
| Non Proprietary Name: | Hydrocortisone Acetate |
| Active Ingredient(s): | 1 g/100g & nbsp; Hydrocortisone Acetate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydrocortisone
| Product NDC: | 37808-929 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100915 |
Package Information of Hydrocortisone
| Package NDC: | 37808-929-64 |
| Package Description: | 1 TUBE in 1 CARTON (37808-929-64) > 28 g in 1 TUBE |
NDC Information of Hydrocortisone
| NDC Code | 37808-929-64 |
| Proprietary Name | Hydrocortisone |
| Package Description | 1 TUBE in 1 CARTON (37808-929-64) > 28 g in 1 TUBE |
| Product NDC | 37808-929 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Hydrocortisone Acetate |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20100915 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | H E B |
| Substance Name | HYDROCORTISONE ACETATE |
| Strength Number | 1 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
