Product NDC: | 63323-282 |
Proprietary Name: | Clindamycin |
Non Proprietary Name: | CLINDAMYCIN PHOSPHATE |
Active Ingredient(s): | 150 mg/mL & nbsp; CLINDAMYCIN PHOSPHATE |
Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63323-282 |
Labeler Name: | APP Pharmaceuticals, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA065347 |
Marketing Category: | ANDA |
Start Marketing Date: | 20091122 |
Package NDC: | 63323-282-06 |
Package Description: | 25 VIAL in 1 TRAY (63323-282-06) > 6 mL in 1 VIAL |
NDC Code | 63323-282-06 |
Proprietary Name | Clindamycin |
Package Description | 25 VIAL in 1 TRAY (63323-282-06) > 6 mL in 1 VIAL |
Product NDC | 63323-282 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | CLINDAMYCIN PHOSPHATE |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 20091122 |
Marketing Category Name | ANDA |
Labeler Name | APP Pharmaceuticals, LLC |
Substance Name | CLINDAMYCIN PHOSPHATE |
Strength Number | 150 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Decreased Sebaceous Gland Activity [PE],Lincosamide Antibacterial [EPC],Lincosamides [Chemical/Ingredient] |