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Hydrocortisone
Hydrocortisone - 51141-0065-1 - (Hydrocortisone)
Drug Information of Hydrocortisone
| Product NDC: | 51141-0065 |
| Proprietary Name: | Hydrocortisone |
| Non Proprietary Name: | Hydrocortisone |
| Active Ingredient(s): | 1 h/100g & nbsp; Hydrocortisone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Hydrocortisone
| Product NDC: | 51141-0065 |
| Labeler Name: | NeoPharm Co., Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100901 |
Package Information of Hydrocortisone
| Package NDC: | 51141-0065-1 |
| Package Description: | 1 TUBE in 1 BOX (51141-0065-1) > 28 g in 1 TUBE |
NDC Information of Hydrocortisone
| NDC Code | 51141-0065-1 |
| Proprietary Name | Hydrocortisone |
| Package Description | 1 TUBE in 1 BOX (51141-0065-1) > 28 g in 1 TUBE |
| Product NDC | 51141-0065 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Hydrocortisone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100901 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | NeoPharm Co., Ltd. |
| Substance Name | HYDROCORTISONE |
| Strength Number | 1 |
| Strength Unit | h/100g |
| Pharmaceutical Classes |
