Product NDC: | 25021-115 |
Proprietary Name: | Clindamycin |
Non Proprietary Name: | Clindamycin Phosphate |
Active Ingredient(s): | 150 mg/mL & nbsp; Clindamycin Phosphate |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 25021-115 |
Labeler Name: | Sagent Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA090109 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120515 |
Package NDC: | 25021-115-02 |
Package Description: | 25 VIAL in 1 CARTON (25021-115-02) > 2 mL in 1 VIAL |
NDC Code | 25021-115-02 |
Proprietary Name | Clindamycin |
Package Description | 25 VIAL in 1 CARTON (25021-115-02) > 2 mL in 1 VIAL |
Product NDC | 25021-115 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Clindamycin Phosphate |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20120515 |
Marketing Category Name | ANDA |
Labeler Name | Sagent Pharmaceuticals |
Substance Name | CLINDAMYCIN PHOSPHATE |
Strength Number | 150 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Decreased Sebaceous Gland Activity [PE],Lincosamide Antibacterial [EPC],Lincosamides [Chemical/Ingredient] |