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DENBLAN
DENBLAN - 16555-996-01 - (SODIUM MONOFLUOROPHOSPHATE)
Drug Information of DENBLAN
| Product NDC: | 16555-996 |
| Proprietary Name: | DENBLAN |
| Non Proprietary Name: | SODIUM MONOFLUOROPHOSPHATE |
| Active Ingredient(s): | .76 mL/100mL & nbsp; SODIUM MONOFLUOROPHOSPHATE |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | PASTE, DENTIFRICE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DENBLAN
| Product NDC: | 16555-996 |
| Labeler Name: | DARPHIN DIST. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20040801 |
Package Information of DENBLAN
| Package NDC: | 16555-996-01 |
| Package Description: | 1 TUBE in 1 CARTON (16555-996-01) > 75 mL in 1 TUBE |
NDC Information of DENBLAN
| NDC Code | 16555-996-01 |
| Proprietary Name | DENBLAN |
| Package Description | 1 TUBE in 1 CARTON (16555-996-01) > 75 mL in 1 TUBE |
| Product NDC | 16555-996 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SODIUM MONOFLUOROPHOSPHATE |
| Dosage Form Name | PASTE, DENTIFRICE |
| Route Name | DENTAL |
| Start Marketing Date | 20040801 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | DARPHIN DIST. |
| Substance Name | SODIUM MONOFLUOROPHOSPHATE |
| Strength Number | .76 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
