Product NDC: | 10922-825 |
Proprietary Name: | Finacea |
Non Proprietary Name: | azelaic acid |
Active Ingredient(s): | .15 g/g & nbsp; azelaic acid |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10922-825 |
Labeler Name: | Intendis Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021470 |
Marketing Category: | NDA |
Start Marketing Date: | 20041224 |
Package NDC: | 10922-825-02 |
Package Description: | 1 TUBE in 1 CARTON (10922-825-02) > 50 g in 1 TUBE |
NDC Code | 10922-825-02 |
Proprietary Name | Finacea |
Package Description | 1 TUBE in 1 CARTON (10922-825-02) > 50 g in 1 TUBE |
Product NDC | 10922-825 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | azelaic acid |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20041224 |
Marketing Category Name | NDA |
Labeler Name | Intendis Inc. |
Substance Name | AZELAIC ACID |
Strength Number | .15 |
Strength Unit | g/g |
Pharmaceutical Classes | Decreased Protein Synthesis [PE],Decreased Sebaceous Gland Activity [PE] |