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BIOTENE
BIOTENE - 0135-0487-01 - (sodium monofluorophosphate)
Drug Information of BIOTENE
| Product NDC: | 0135-0487 |
| Proprietary Name: | BIOTENE |
| Non Proprietary Name: | sodium monofluorophosphate |
| Active Ingredient(s): | 1.4 mg/g & nbsp; sodium monofluorophosphate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | PASTE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of BIOTENE
| Product NDC: | 0135-0487 |
| Labeler Name: | GlaxoSmithKline Consumer Healthcare LP |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part355 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110418 |
Package Information of BIOTENE
| Package NDC: | 0135-0487-01 |
| Package Description: | 1 TUBE in 1 CARTON (0135-0487-01) > 127.6 g in 1 TUBE |
NDC Information of BIOTENE
| NDC Code | 0135-0487-01 |
| Proprietary Name | BIOTENE |
| Package Description | 1 TUBE in 1 CARTON (0135-0487-01) > 127.6 g in 1 TUBE |
| Product NDC | 0135-0487 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | sodium monofluorophosphate |
| Dosage Form Name | PASTE |
| Route Name | ORAL |
| Start Marketing Date | 20110418 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | GlaxoSmithKline Consumer Healthcare LP |
| Substance Name | SODIUM MONOFLUOROPHOSPHATE |
| Strength Number | 1.4 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
