Product NDC: | 75949-4001 |
Proprietary Name: | ELCURE AC-LEX Serum |
Non Proprietary Name: | AZELAIC ACID |
Active Ingredient(s): | 2.5 mL/50mL & nbsp; AZELAIC ACID |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 75949-4001 |
Labeler Name: | Elcure Co., Ltd. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20111124 |
Package NDC: | 75949-4001-1 |
Package Description: | 50 mL in 1 BOTTLE, GLASS (75949-4001-1) |
NDC Code | 75949-4001-1 |
Proprietary Name | ELCURE AC-LEX Serum |
Package Description | 50 mL in 1 BOTTLE, GLASS (75949-4001-1) |
Product NDC | 75949-4001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | AZELAIC ACID |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20111124 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Elcure Co., Ltd. |
Substance Name | AZELAIC ACID |
Strength Number | 2.5 |
Strength Unit | mL/50mL |
Pharmaceutical Classes |