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Latrix
Latrix - 58980-777-10 - (Urea)
Drug Information of Latrix
| Product NDC: | 58980-777 |
| Proprietary Name: | Latrix |
| Non Proprietary Name: | Urea |
| Active Ingredient(s): | 142 g/284g & nbsp; Urea |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Latrix
| Product NDC: | 58980-777 |
| Labeler Name: | Stratus Pharmaceuticals, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED OTHER |
| Start Marketing Date: | 20081014 |
Package Information of Latrix
| Package NDC: | 58980-777-10 |
| Package Description: | 1 TUBE in 1 BOX (58980-777-10) > 284 g in 1 TUBE |
NDC Information of Latrix
| NDC Code | 58980-777-10 |
| Proprietary Name | Latrix |
| Package Description | 1 TUBE in 1 BOX (58980-777-10) > 284 g in 1 TUBE |
| Product NDC | 58980-777 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Urea |
| Dosage Form Name | SUSPENSION |
| Route Name | TOPICAL |
| Start Marketing Date | 20081014 |
| Marketing Category Name | UNAPPROVED OTHER |
| Labeler Name | Stratus Pharmaceuticals, Inc |
| Substance Name | UREA |
| Strength Number | 142 |
| Strength Unit | g/284g |
| Pharmaceutical Classes |
