salsalate

Generic: salsalate

Labeler: westminster pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name salsalate
Generic Name salsalate
Labeler westminster pharmaceuticals, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

salsalate 750 mg/1

Manufacturer
Westminster Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 69367-616
Product ID 69367-616_56747829-5049-405d-8d69-83c34d70002b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2023-11-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69367616
Hyphenated Format 69367-616

Supplemental Identifiers

RxCUI
312899 583170
UPC
0369367615013 0369367616010
UNII
V9MO595C9I

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name salsalate (source: ndc)
Generic Name salsalate (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (69367-616-01)
source: ndc

Packages (1)

69367-616-01 100 TABLET in 1 BOTTLE (69367-616-01)

Ingredients (1)

salsalate (750 mg/1)

Linked Drug Pages (1)

Salsalate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "56747829-5049-405d-8d69-83c34d70002b", "openfda": {"upc": ["0369367615013", "0369367616010"], "unii": ["V9MO595C9I"], "rxcui": ["312899", "583170"], "spl_set_id": ["24815546-658b-4b01-ac11-de7fbd0ebd16"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69367-616-01)", "package_ndc": "69367-616-01", "marketing_start_date": "20231115"}], "brand_name": "Salsalate", "product_id": "69367-616_56747829-5049-405d-8d69-83c34d70002b", "dosage_form": "TABLET", "product_ndc": "69367-616", "generic_name": "Salsalate", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Salsalate", "active_ingredients": [{"name": "SALSALATE", "strength": "750 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20231115", "listing_expiration_date": "20261231"}