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Urea
Urea - 0168-0646-10 - (urea)
Drug Information of Urea
| Product NDC: | 0168-0646 |
| Proprietary Name: | Urea |
| Non Proprietary Name: | urea |
| Active Ingredient(s): | 500 mg/g & nbsp; urea |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | EMULSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Urea
| Product NDC: | 0168-0646 |
| 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: | 20090901 |
Package Information of Urea
| Package NDC: | 0168-0646-10 |
| Package Description: | 1 TUBE in 1 CARTON (0168-0646-10) > 283.59 g in 1 TUBE |
NDC Information of Urea
| NDC Code | 0168-0646-10 |
| Proprietary Name | Urea |
| Package Description | 1 TUBE in 1 CARTON (0168-0646-10) > 283.59 g in 1 TUBE |
| Product NDC | 0168-0646 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | urea |
| Dosage Form Name | EMULSION |
| Route Name | TOPICAL |
| Start Marketing Date | 20090901 |
| 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 |
