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Eurax
Eurax - 10631-091-60 - (Eurax)
Drug Information of Eurax
| Product NDC: | 10631-091 |
| Proprietary Name: | Eurax |
| Non Proprietary Name: | Eurax |
| Active Ingredient(s): | 100 mg/g & nbsp; Eurax |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Eurax
| Product NDC: | 10631-091 |
| Labeler Name: | Ranbaxy Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA006927 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20081215 |
Package Information of Eurax
| Package NDC: | 10631-091-60 |
| Package Description: | 60 g in 1 TUBE (10631-091-60) |
NDC Information of Eurax
| NDC Code | 10631-091-60 |
| Proprietary Name | Eurax |
| Package Description | 60 g in 1 TUBE (10631-091-60) |
| Product NDC | 10631-091 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Eurax |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20081215 |
| Marketing Category Name | NDA |
| Labeler Name | Ranbaxy Laboratories Inc. |
| Substance Name | CROTAMITON |
| Strength Number | 100 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
