Product NDC: | 68788-9841 |
Proprietary Name: | Clindamycin Phosphate |
Non Proprietary Name: | Clindamycin Phosphate |
Active Ingredient(s): | 20 mg/g & nbsp; Clindamycin Phosphate |
Administration Route(s): | VAGINAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68788-9841 |
Labeler Name: | Preferred Pharmaceuticals, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA065139 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120329 |
Package NDC: | 68788-9841-4 |
Package Description: | 40 g in 1 TUBE, WITH APPLICATOR (68788-9841-4) |
NDC Code | 68788-9841-4 |
Proprietary Name | Clindamycin Phosphate |
Package Description | 40 g in 1 TUBE, WITH APPLICATOR (68788-9841-4) |
Product NDC | 68788-9841 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Clindamycin Phosphate |
Dosage Form Name | CREAM |
Route Name | VAGINAL |
Start Marketing Date | 20120329 |
Marketing Category Name | ANDA |
Labeler Name | Preferred Pharmaceuticals, Inc |
Substance Name | CLINDAMYCIN PHOSPHATE |
Strength Number | 20 |
Strength Unit | mg/g |
Pharmaceutical Classes | Decreased Sebaceous Gland Activity [PE],Lincosamide Antibacterial [EPC],Lincosamides [Chemical/Ingredient] |