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Apatite
Apatite - 76058-102-02 - (SODIUM MONOFLUOROPHOSPHATE)
Drug Information of Apatite
| Product NDC: | 76058-102 |
| Proprietary Name: | Apatite |
| Non Proprietary Name: | SODIUM MONOFLUOROPHOSPHATE |
| Active Ingredient(s): | 1380 mg/200g & nbsp; SODIUM MONOFLUOROPHOSPHATE |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Apatite
| Product NDC: | 76058-102 |
| Labeler Name: | Sungwon Pharmaceutical Co., Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110301 |
Package Information of Apatite
| Package NDC: | 76058-102-02 |
| Package Description: | 1 TUBE in 1 CARTON (76058-102-02) > 200 g in 1 TUBE (76058-102-01) |
NDC Information of Apatite
| NDC Code | 76058-102-02 |
| Proprietary Name | Apatite |
| Package Description | 1 TUBE in 1 CARTON (76058-102-02) > 200 g in 1 TUBE (76058-102-01) |
| Product NDC | 76058-102 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM MONOFLUOROPHOSPHATE |
| Dosage Form Name | PASTE, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20110301 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Sungwon Pharmaceutical Co., Ltd. |
| Substance Name | SODIUM MONOFLUOROPHOSPHATE |
| Strength Number | 1380 |
| Strength Unit | mg/200g |
| Pharmaceutical Classes |
