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Urea
Urea - 42192-707-18 - (Urea)
Drug Information of Urea
| Product NDC: | 42192-707 |
| Proprietary Name: | Urea |
| Non Proprietary Name: | Urea |
| Active Ingredient(s): | 400 mg/g & nbsp; Urea |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Urea
| Product NDC: | 42192-707 |
| Labeler Name: | Acella Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20090622 |
Package Information of Urea
| Package NDC: | 42192-707-18 |
| Package Description: | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (42192-707-18) > 18 g in 1 BOTTLE, WITH APPLICATOR |
NDC Information of Urea
| NDC Code | 42192-707-18 |
| Proprietary Name | Urea |
| Package Description | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (42192-707-18) > 18 g in 1 BOTTLE, WITH APPLICATOR |
| Product NDC | 42192-707 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Urea |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20090622 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Acella Pharmaceuticals, LLC |
| Substance Name | UREA |
| Strength Number | 400 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
