| Product NDC: | 59762-3743 |
| Proprietary Name: | clindamycin phosphate |
| Non Proprietary Name: | clindamycin phosphate |
| Active Ingredient(s): | 10 mg/g & nbsp; clindamycin phosphate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 59762-3743 |
| Labeler Name: | Greenstone LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050615 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 19870107 |
| Package NDC: | 59762-3743-1 |
| Package Description: | 30 g in 1 TUBE (59762-3743-1) |
| NDC Code | 59762-3743-1 |
| Proprietary Name | clindamycin phosphate |
| Package Description | 30 g in 1 TUBE (59762-3743-1) |
| Product NDC | 59762-3743 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | clindamycin phosphate |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 19870107 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Greenstone LLC |
| Substance Name | CLINDAMYCIN PHOSPHATE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Decreased Sebaceous Gland Activity [PE],Lincosamide Antibacterial [EPC],Lincosamides [Chemical/Ingredient] |