Product NDC: | 0781-3289 |
Proprietary Name: | Clindamycin in 5 Percent Dextrose |
Non Proprietary Name: | Clindamycin in 5 Percent Dextrose |
Active Ingredient(s): | 12 mg/mL & nbsp; Clindamycin in 5 Percent Dextrose |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0781-3289 |
Labeler Name: | Sandoz Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA201692 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130207 |
Package NDC: | 0781-3289-09 |
Package Description: | 24 BAG in 1 CARTON (0781-3289-09) > 50 mL in 1 BAG (0781-3289-91) |
NDC Code | 0781-3289-09 |
Proprietary Name | Clindamycin in 5 Percent Dextrose |
Package Description | 24 BAG in 1 CARTON (0781-3289-09) > 50 mL in 1 BAG (0781-3289-91) |
Product NDC | 0781-3289 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Clindamycin in 5 Percent Dextrose |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20130207 |
Marketing Category Name | ANDA |
Labeler Name | Sandoz Inc |
Substance Name | CLINDAMYCIN |
Strength Number | 12 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Decreased Sebaceous Gland Activity [PE],Lincosamide Antibacterial [EPC],Lincosamides [Chemical/Ingredient] |