| Product NDC: | 66467-2560 |
| Proprietary Name: | Superdent |
| Non Proprietary Name: | Chlorhexidine Gluconate |
| Active Ingredient(s): | .12 g/mL & nbsp; Chlorhexidine Gluconate |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 66467-2560 |
| Labeler Name: | Darby Dental Supply Co Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077789 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060702 |
| Package NDC: | 66467-2560-1 |
| Package Description: | 473 mL in 1 BOTTLE, PLASTIC (66467-2560-1) |
| NDC Code | 66467-2560-1 |
| Proprietary Name | Superdent |
| Package Description | 473 mL in 1 BOTTLE, PLASTIC (66467-2560-1) |
| Product NDC | 66467-2560 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Chlorhexidine Gluconate |
| Dosage Form Name | LIQUID |
| Route Name | DENTAL |
| Start Marketing Date | 20060702 |
| Marketing Category Name | ANDA |
| Labeler Name | Darby Dental Supply Co Inc |
| Substance Name | CHLORHEXIDINE GLUCONATE |
| Strength Number | .12 |
| Strength Unit | g/mL |
| Pharmaceutical Classes | Decreased Cell Wall Integrity [PE] |