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] |