Product NDC: | 59762-5009 |
Proprietary Name: | clindamycin phosphate |
Non Proprietary Name: | CLINDAMYCIN PHOSPHATE |
Active Ingredient(s): | 20 mg/g & nbsp; CLINDAMYCIN PHOSPHATE |
Administration Route(s): | VAGINAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59762-5009 |
Labeler Name: | Greenstone LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA050680 |
Marketing Category: | NDA AUTHORIZED GENERIC |
Start Marketing Date: | 19920811 |
Package NDC: | 59762-5009-1 |
Package Description: | 1 TUBE in 1 CARTON (59762-5009-1) > 40 g in 1 TUBE |
NDC Code | 59762-5009-1 |
Proprietary Name | clindamycin phosphate |
Package Description | 1 TUBE in 1 CARTON (59762-5009-1) > 40 g in 1 TUBE |
Product NDC | 59762-5009 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | CLINDAMYCIN PHOSPHATE |
Dosage Form Name | CREAM |
Route Name | VAGINAL |
Start Marketing Date | 19920811 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Labeler Name | Greenstone LLC |
Substance Name | CLINDAMYCIN PHOSPHATE |
Strength Number | 20 |
Strength Unit | mg/g |
Pharmaceutical Classes | Decreased Sebaceous Gland Activity [PE],Lincosamide Antibacterial [EPC],Lincosamides [Chemical/Ingredient] |