Ludent is a Oral Tablet, Chewable in the Human Prescription Drug category. It is labeled and distributed by Sancilio & Company Inc. The primary component is Sodium Fluoride.
Product ID | 44946-1016_3424acc5-d8d6-4d35-b83e-f89323bbc289 |
NDC | 44946-1016 |
Product Type | Human Prescription Drug |
Proprietary Name | Ludent |
Generic Name | Sodium Fluoride |
Dosage Form | Tablet, Chewable |
Route of Administration | ORAL |
Marketing Start Date | 2009-09-10 |
Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
Labeler Name | Sancilio & Company Inc |
Substance Name | SODIUM FLUORIDE |
Active Ingredient Strength | 1 mg/1 |
NDC Exclude Flag | E |
Listing Certified Through | 2017-12-31 |
Marketing Start Date | 2009-09-10 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | Unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-09-10 |
Inactivation Date | 2019-10-21 |
Marketing Category | Unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-09-10 |
Inactivation Date | 2019-10-21 |
Marketing Category | Unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-09-10 |
Inactivation Date | 2019-10-21 |
Marketing Category | Unapproved drug other |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2009-09-10 |
Inactivation Date | 2019-10-21 |
Ingredient | Strength |
---|---|
SODIUM FLUORIDE | .5 mg/1 |
SPL SET ID: | 6e7a7e17-7538-4763-810c-7e56bd630494 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
44946-1016 | Ludent | Ludent |
44946-1017 | Ludent | Ludent |
44946-1015 | Ludent | Ludent |
0135-0234 | AQUAFRESH | sodium fluoride |
0126-0021 | Colgate | SODIUM FLUORIDE |
0126-0034 | Colgate Phos-Flur Ortho Defense Alcohol Free Anticavity Gushing Grape Fluoride | SODIUM FLUORIDE |
0126-0032 | Colgate Phos-Flur Ortho Defense Alcohol Free Anticavity Mint Fluoride | SODIUM FLUORIDE |
0041-1421 | Oral-B | Sodium Fluoride |
0126-0131 | Phos-Flur | Sodium Fluoride |
0126-0135 | Phos-Flur Ortho Defense | SODIUM FLUORIDE |
0126-0138 | Phos-Flur Ortho Defense | SODIUM FLUORIDE |
0126-0139 | Phos-Flur Ortho Defense | SODIUM FLUORIDE |
0126-0074 | PrevidDent 5000 Booster Plus Spearmint | Sodium Fluoride |
0126-0016 | PreviDent | Sodium fluoride |
0126-0075 | PreviDent | Sodium fluoride |
0126-0076 | PreviDent | Sodium fluoride |
0126-0179 | PreviDent | Sodium Fluoride |
0126-0286 | PreviDent | Sodium Fluoride |
0126-0287 | PreviDent | Sodium Fluoride |
0126-0072 | PreviDent 5000 Booster Plus Fruitastic | Sodium Fluoride |
0126-0033 | PreviDent Alcohol Free | Sodium Fluoride |
0126-0088 | PreviDent Fresh Mint | Sodium Fluoride |
0126-0289 | PreviDent OrthoDefense | SODIUM FLUORIDE |
0126-0288 | PreviDent Very Berry | Sodium Fluoride |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
LUDENT 98004788 not registered Live/Pending |
Luvantix ADM Co., Ltd. 2023-05-19 |
LUDENT 98004788 not registered Live/Pending |
3DMaterials Co., Ltd. 2023-05-19 |
LUDENT 77865700 3869394 Live/Registered |
MICELLE BIOPHARMA, INC. 2009-11-05 |