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NEW DOCTOR AG PLUS
NEW DOCTOR AG PLUS - 75984-001-01 - (SODIUM MONOFLUOROPHOSPHATE)
Drug Information of NEW DOCTOR AG PLUS
| Product NDC: | 75984-001 |
| Proprietary Name: | NEW DOCTOR AG PLUS |
| Non Proprietary Name: | SODIUM MONOFLUOROPHOSPHATE |
| Active Ingredient(s): | .15 g/150g & nbsp; SODIUM MONOFLUOROPHOSPHATE |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NEW DOCTOR AG PLUS
| Product NDC: | 75984-001 |
| Labeler Name: | HANIL PHARMACEUTICAL CO., LTD. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100901 |
Package Information of NEW DOCTOR AG PLUS
| Package NDC: | 75984-001-01 |
| Package Description: | 150 g in 1 CARTON (75984-001-01) |
NDC Information of NEW DOCTOR AG PLUS
| NDC Code | 75984-001-01 |
| Proprietary Name | NEW DOCTOR AG PLUS |
| Package Description | 150 g in 1 CARTON (75984-001-01) |
| Product NDC | 75984-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM MONOFLUOROPHOSPHATE |
| Dosage Form Name | PASTE, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20100901 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | HANIL PHARMACEUTICAL CO., LTD. |
| Substance Name | SODIUM MONOFLUOROPHOSPHATE |
| Strength Number | .15 |
| Strength Unit | g/150g |
| Pharmaceutical Classes |
