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Denpo
Denpo - 52146-1001-1 - (fluoride)
Drug Information of Denpo
| Product NDC: | 52146-1001 |
| Proprietary Name: | Denpo |
| Non Proprietary Name: | fluoride |
| Active Ingredient(s): | 1.1 mg/1 & nbsp; fluoride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, CHEWABLE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Denpo
| Product NDC: | 52146-1001 |
| Labeler Name: | Suheung Capsule Co., Ltd |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100318 |
Package Information of Denpo
| Package NDC: | 52146-1001-1 |
| Package Description: | 60 TABLET, CHEWABLE in 1 PACKAGE (52146-1001-1) |
NDC Information of Denpo
| NDC Code | 52146-1001-1 |
| Proprietary Name | Denpo |
| Package Description | 60 TABLET, CHEWABLE in 1 PACKAGE (52146-1001-1) |
| Product NDC | 52146-1001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | fluoride |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 20100318 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Suheung Capsule Co., Ltd |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | 1.1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
