Product NDC: | 21695-763 |
Proprietary Name: | Tretinoin |
Non Proprietary Name: | tretinoin |
Active Ingredient(s): | .25 mg/g & nbsp; tretinoin |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 21695-763 |
Labeler Name: | Rebel Distributors Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075529 |
Marketing Category: | ANDA |
Start Marketing Date: | 20000222 |
Package NDC: | 21695-763-15 |
Package Description: | 1 TUBE in 1 CARTON (21695-763-15) > 15 g in 1 TUBE |
NDC Code | 21695-763-15 |
Proprietary Name | Tretinoin |
Package Description | 1 TUBE in 1 CARTON (21695-763-15) > 15 g in 1 TUBE |
Product NDC | 21695-763 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | tretinoin |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20000222 |
Marketing Category Name | ANDA |
Labeler Name | Rebel Distributors Corp |
Substance Name | TRETINOIN |
Strength Number | .25 |
Strength Unit | mg/g |
Pharmaceutical Classes | Retinoid [EPC],Retinoids [Chemical/Ingredient] |