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Umecta PD
Umecta PD - 68712-017-02 - (Urea)
Drug Information of Umecta PD
| Product NDC: | 68712-017 |
| Proprietary Name: | Umecta PD |
| Non Proprietary Name: | Urea |
| Active Ingredient(s): | 400 mg/g & nbsp; Urea |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | EMULSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Umecta PD
| Product NDC: | 68712-017 |
| Labeler Name: | Innocutis Holdings LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20070601 |
Package Information of Umecta PD
| Package NDC: | 68712-017-02 |
| Package Description: | 198.5 g in 1 BOTTLE (68712-017-02) |
NDC Information of Umecta PD
| NDC Code | 68712-017-02 |
| Proprietary Name | Umecta PD |
| Package Description | 198.5 g in 1 BOTTLE (68712-017-02) |
| Product NDC | 68712-017 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Urea |
| Dosage Form Name | EMULSION |
| Route Name | TOPICAL |
| Start Marketing Date | 20070601 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Innocutis Holdings LLC |
| Substance Name | UREA |
| Strength Number | 400 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
