Salsalate
- Product NDC
- 13273-209
- 11-digit product format
- 132730209
- Labeler code
- 13273
- Product ID
- 13273-209_f65890ab-7296-4194-972b-98ff9637fc7c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Salsalate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- ANDAPharm LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2015-01-01
- Marketing end
- 0000-00-00
- Substance
- SALSALATE
- Active strength
- 500 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 13273-209-03 | Salsalate Rx | 100 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 100 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 13273-209 | SALSALATE RX (SALSALATE) TABLET, FILM COATED [ANDAPHARM LLC] | 1 | Legacy NDC, 1 package rows | 20150217_a51b97ac-1881-4ade-8b37-86c1c092eb1e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 13273-209-03 | 13273020903 | 100 in 1 BOTTLE, PLASTIC | Historical |