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Natureplex Hydrocortisone
Natureplex Hydrocortisone - 67234-010-01 - (Hydrocortisone)
Drug Information of Natureplex Hydrocortisone
| Product NDC: | 67234-010 |
| Proprietary Name: | Natureplex Hydrocortisone |
| Non Proprietary Name: | Hydrocortisone |
| Active Ingredient(s): | .01 g/g & nbsp; Hydrocortisone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Natureplex Hydrocortisone
| Product NDC: | 67234-010 |
| Labeler Name: | Natureplex, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20080122 |
Package Information of Natureplex Hydrocortisone
| Package NDC: | 67234-010-01 |
| Package Description: | 28 g in 1 TUBE (67234-010-01) |
NDC Information of Natureplex Hydrocortisone
| NDC Code | 67234-010-01 |
| Proprietary Name | Natureplex Hydrocortisone |
| Package Description | 28 g in 1 TUBE (67234-010-01) |
| Product NDC | 67234-010 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Hydrocortisone |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20080122 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Natureplex, LLC |
| Substance Name | HYDROCORTISONE |
| Strength Number | .01 |
| Strength Unit | g/g |
| Pharmaceutical Classes |
