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Darby
Darby - 66467-2170-1 - (Sodium Fluoride)
Drug Information of Darby
| Product NDC: | 66467-2170 |
| Proprietary Name: | Darby |
| Non Proprietary Name: | Sodium Fluoride |
| Active Ingredient(s): | .0272 g/mL & nbsp; Sodium Fluoride |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Darby
| Product NDC: | 66467-2170 |
| Labeler Name: | Darby Dental Supply Co Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20101112 |
Package Information of Darby
| Package NDC: | 66467-2170-1 |
| Package Description: | 480 mL in 1 BOTTLE, PLASTIC (66467-2170-1) |
NDC Information of Darby
| NDC Code | 66467-2170-1 |
| Proprietary Name | Darby |
| Package Description | 480 mL in 1 BOTTLE, PLASTIC (66467-2170-1) |
| Product NDC | 66467-2170 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Fluoride |
| Dosage Form Name | GEL |
| Route Name | DENTAL |
| Start Marketing Date | 20101112 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Darby Dental Supply Co Inc |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | .0272 |
| Strength Unit | g/mL |
| Pharmaceutical Classes |
