Product NDC: | 0168-0493 |
Proprietary Name: | Urea |
Non Proprietary Name: | urea |
Active Ingredient(s): | 500 mg/g & nbsp; urea |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0168-0493 |
Labeler Name: | E. FOUGERA & CO., A division of Nycomed US Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED OTHER |
Start Marketing Date: | 20090915 |
Package NDC: | 0168-0493-84 |
Package Description: | 284 g in 1 TUBE (0168-0493-84) |
NDC Code | 0168-0493-84 |
Proprietary Name | Urea |
Package Description | 284 g in 1 TUBE (0168-0493-84) |
Product NDC | 0168-0493 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | urea |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 20090915 |
Marketing Category Name | UNAPPROVED OTHER |
Labeler Name | E. FOUGERA & CO., A division of Nycomed US Inc. |
Substance Name | UREA |
Strength Number | 500 |
Strength Unit | mg/g |
Pharmaceutical Classes |