Product NDC: | 51672-4081 |
Proprietary Name: | Clindamycin Phosphate |
Non Proprietary Name: | Clindamycin phosphate |
Active Ingredient(s): | 10 mg/mL & nbsp; Clindamycin phosphate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51672-4081 |
Labeler Name: | Taro Pharmaceuticals U.S.A., Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA065184 |
Marketing Category: | ANDA |
Start Marketing Date: | 20040331 |
Package NDC: | 51672-4081-3 |
Package Description: | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (51672-4081-3) > 30 mL in 1 BOTTLE, WITH APPLICATOR |
NDC Code | 51672-4081-3 |
Proprietary Name | Clindamycin Phosphate |
Package Description | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (51672-4081-3) > 30 mL in 1 BOTTLE, WITH APPLICATOR |
Product NDC | 51672-4081 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Clindamycin phosphate |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 20040331 |
Marketing Category Name | ANDA |
Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
Substance Name | CLINDAMYCIN PHOSPHATE |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Decreased Sebaceous Gland Activity [PE],Lincosamide Antibacterial [EPC],Lincosamides [Chemical/Ingredient] |