Salsalate
- Product NDC
- 50682-507
- 11-digit product format
- 506820507
- Labeler code
- 50682
- Product ID
- 50682-507_409093a5-b4f0-4857-b3d6-3d40481511d4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Salsalate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- 3T Federal Solutions LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2012-01-16
- Marketing end
- 0000-00-00
- Substance
- SALSALATE
- Active strength
- 500 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50682-507-01 | Salsalate | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 1 |
| 50682-507-05 | Salsalate | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | | 1 |
| 50682-507-10 | Salsalate | 1000 in 1 BOTTLE | TABLET, FILM COATED | 1000 | | 1 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| SALSALATE | ACTIVE INGREDIENT | V9MO595C9I | SALSALATE TABLET, FILM COATED [3T FEDERAL SOLUTIONS LLC] | 1 | |
| SALSALATE | ACTIVE MOIETY | V9MO595C9I | SALSALATE TABLET, FILM COATED [3T FEDERAL SOLUTIONS LLC] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | SALSALATE TABLET, FILM COATED [3T FEDERAL SOLUTIONS LLC] | 1 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | SALSALATE TABLET, FILM COATED [3T FEDERAL SOLUTIONS LLC] | 1 | |
| D&C YELLOW NO. 10 | INACTIVE INGREDIENT | 35SW5USQ3G | SALSALATE TABLET, FILM COATED [3T FEDERAL SOLUTIONS LLC] | 1 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | SALSALATE TABLET, FILM COATED [3T FEDERAL SOLUTIONS LLC] | 1 | |
| MINERAL OIL | INACTIVE INGREDIENT | T5L8T28FGP | SALSALATE TABLET, FILM COATED [3T FEDERAL SOLUTIONS LLC] | 1 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | SALSALATE TABLET, FILM COATED [3T FEDERAL SOLUTIONS LLC] | 1 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | SALSALATE TABLET, FILM COATED [3T FEDERAL SOLUTIONS LLC] | 1 | |
| STEARIC ACID | INACTIVE INGREDIENT | 4ELV7Z65AP | SALSALATE TABLET, FILM COATED [3T FEDERAL SOLUTIONS LLC] | 1 | |
| TALC | INACTIVE INGREDIENT | 7SEV7J4R1U | SALSALATE TABLET, FILM COATED [3T FEDERAL SOLUTIONS LLC] | 1 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | SALSALATE TABLET, FILM COATED [3T FEDERAL SOLUTIONS LLC] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50682-507 | SALSALATE TABLET, FILM COATED [3T FEDERAL SOLUTIONS LLC] | 1 | Legacy NDC, 3 package rows | 20120411_2ada2b3c-afcf-44bd-b0b8-bd4a1bc5673a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50682-507-01 | 50682050701 | 100 in 1 BOTTLE | Historical |
| 50682-507-05 | 50682050705 | 500 in 1 BOTTLE | Historical |
| 50682-507-10 | 50682050710 | 1000 in 1 BOTTLE | Historical |