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Urea
Urea - 51862-181-28 - (Urea)
Drug Information of Urea
| Product NDC: | 51862-181 |
| Proprietary Name: | Urea |
| Non Proprietary Name: | Urea |
| Active Ingredient(s): | 450 mg/g & nbsp; Urea |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Urea
| Product NDC: | 51862-181 |
| Labeler Name: | Libertas Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20111028 |
Package Information of Urea
| Package NDC: | 51862-181-28 |
| Package Description: | 1 BOTTLE, GLASS in 1 CARTON (51862-181-28) > 28 g in 1 BOTTLE, GLASS |
NDC Information of Urea
| NDC Code | 51862-181-28 |
| Proprietary Name | Urea |
| Package Description | 1 BOTTLE, GLASS in 1 CARTON (51862-181-28) > 28 g in 1 BOTTLE, GLASS |
| Product NDC | 51862-181 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Urea |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20111028 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Libertas Pharma, Inc. |
| Substance Name | UREA |
| Strength Number | 450 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
