Product NDC: | 54868-5833 |
Proprietary Name: | Cleocin |
Non Proprietary Name: | clindamycin palmitate hydrochloride |
Active Ingredient(s): | 75 mg/5mL & nbsp; clindamycin palmitate hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | GRANULE, FOR SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-5833 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA061772 |
Marketing Category: | ANDA |
Start Marketing Date: | 20071128 |
Package NDC: | 54868-5833-0 |
Package Description: | 100 mL in 1 BOTTLE (54868-5833-0) |
NDC Code | 54868-5833-0 |
Proprietary Name | Cleocin |
Package Description | 100 mL in 1 BOTTLE (54868-5833-0) |
Product NDC | 54868-5833 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | clindamycin palmitate hydrochloride |
Dosage Form Name | GRANULE, FOR SOLUTION |
Route Name | ORAL |
Start Marketing Date | 20071128 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | CLINDAMYCIN PALMITATE HYDROCHLORIDE |
Strength Number | 75 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Decreased Sebaceous Gland Activity [PE],Lincosamide Antibacterial [EPC],Lincosamides [Chemical/Ingredient] |