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UREA - 42192-101-10 - (UREA)
Drug Information of UREA
| Product NDC: | 42192-101 |
| Proprietary Name: | UREA |
| Non Proprietary Name: | UREA |
| Active Ingredient(s): | 50 g/100g & nbsp; UREA |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | EMULSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of UREA
| Product NDC: | 42192-101 |
| Labeler Name: | ACELLA PHARMACEUTICALS |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20101108 |
Package Information of UREA
| Package NDC: | 42192-101-10 |
| Package Description: | 283.5 g in 1 TUBE (42192-101-10) |
NDC Information of UREA
| NDC Code | 42192-101-10 |
| Proprietary Name | UREA |
| Package Description | 283.5 g in 1 TUBE (42192-101-10) |
| Product NDC | 42192-101 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | UREA |
| Dosage Form Name | EMULSION |
| Route Name | TOPICAL |
| Start Marketing Date | 20101108 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | ACELLA PHARMACEUTICALS |
| Substance Name | UREA |
| Strength Number | 50 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
