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Westcort
Westcort - 10631-105-15 - (Hydrocortisone valerate)
Drug Information of Westcort
| Product NDC: | 10631-105 |
| Proprietary Name: | Westcort |
| Non Proprietary Name: | Hydrocortisone valerate |
| Active Ingredient(s): | 2 mg/g & nbsp; Hydrocortisone valerate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Westcort
| Product NDC: | 10631-105 |
| Labeler Name: | Ranbaxy Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018726 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20081006 |
Package Information of Westcort
| Package NDC: | 10631-105-15 |
| Package Description: | 15 g in 1 TUBE (10631-105-15) |
NDC Information of Westcort
| NDC Code | 10631-105-15 |
| Proprietary Name | Westcort |
| Package Description | 15 g in 1 TUBE (10631-105-15) |
| Product NDC | 10631-105 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydrocortisone valerate |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20081006 |
| Marketing Category Name | NDA |
| Labeler Name | Ranbaxy Laboratories Inc. |
| Substance Name | HYDROCORTISONE VALERATE |
| Strength Number | 2 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
