Product NDC: | 0062-0190 |
Proprietary Name: | Retin-A MICRO |
Non Proprietary Name: | Tretinoin |
Active Ingredient(s): | .1 mg/g & nbsp; Tretinoin |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0062-0190 |
Labeler Name: | Ortho-McNeil Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020475 |
Marketing Category: | NDA |
Start Marketing Date: | 20110501 |
Package NDC: | 0062-0190-02 |
Package Description: | 1 TUBE in 1 CARTON (0062-0190-02) > 20 g in 1 TUBE |
NDC Code | 0062-0190-02 |
Proprietary Name | Retin-A MICRO |
Package Description | 1 TUBE in 1 CARTON (0062-0190-02) > 20 g in 1 TUBE |
Product NDC | 0062-0190 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Tretinoin |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20110501 |
Marketing Category Name | NDA |
Labeler Name | Ortho-McNeil Pharmaceuticals |
Substance Name | TRETINOIN |
Strength Number | .1 |
Strength Unit | mg/g |
Pharmaceutical Classes | Retinoid [EPC],Retinoids [Chemical/Ingredient] |