Product NDC: | 68788-9833 |
Proprietary Name: | Tretinoin |
Non Proprietary Name: | tretinoin |
Active Ingredient(s): | 1 mg/g & nbsp; tretinoin |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68788-9833 |
Labeler Name: | Preferred Pharmaceuticals, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075213 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120329 |
Package NDC: | 68788-9833-2 |
Package Description: | 20 g in 1 TUBE (68788-9833-2) |
NDC Code | 68788-9833-2 |
Proprietary Name | Tretinoin |
Package Description | 20 g in 1 TUBE (68788-9833-2) |
Product NDC | 68788-9833 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | tretinoin |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20120329 |
Marketing Category Name | ANDA |
Labeler Name | Preferred Pharmaceuticals, Inc |
Substance Name | TRETINOIN |
Strength Number | 1 |
Strength Unit | mg/g |
Pharmaceutical Classes | Retinoid [EPC],Retinoids [Chemical/Ingredient] |