Product NDC: | 13548-638 |
Proprietary Name: | Refissa |
Non Proprietary Name: | Tretinoin |
Active Ingredient(s): | .5 mg/g & nbsp; Tretinoin |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 13548-638 |
Labeler Name: | Coria Laboratories, LTD |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076498 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110201 |
Package NDC: | 13548-638-40 |
Package Description: | 40 g in 1 TUBE (13548-638-40) |
NDC Code | 13548-638-40 |
Proprietary Name | Refissa |
Package Description | 40 g in 1 TUBE (13548-638-40) |
Product NDC | 13548-638 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Tretinoin |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20110201 |
Marketing Category Name | ANDA |
Labeler Name | Coria Laboratories, LTD |
Substance Name | TRETINOIN |
Strength Number | .5 |
Strength Unit | mg/g |
Pharmaceutical Classes | Retinoid [EPC],Retinoids [Chemical/Ingredient] |