BIOTENE - 0135-0487-01 - (sodium monofluorophosphate)

Alphabetical Index


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

Complete Information of BIOTENE


General Information