Product NDC: | 21695-888 |
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: | 21695-888 |
Labeler Name: | Rebel Distributors Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA064159 |
Marketing Category: | ANDA |
Start Marketing Date: | 19970605 |
Package NDC: | 21695-888-60 |
Package Description: | 60 PACKET in 1 CARTON (21695-888-60) > 1 mL in 1 PACKET |
NDC Code | 21695-888-60 |
Proprietary Name | Clindamycin Phosphate |
Package Description | 60 PACKET in 1 CARTON (21695-888-60) > 1 mL in 1 PACKET |
Product NDC | 21695-888 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Clindamycin Phosphate |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 19970605 |
Marketing Category Name | ANDA |
Labeler Name | Rebel Distributors Corp |
Substance Name | CLINDAMYCIN PHOSPHATE |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Decreased Sebaceous Gland Activity [PE],Lincosamide Antibacterial [EPC],Lincosamides [Chemical/Ingredient] |