sulfasalazine
Generic: sulfasalazine
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
sulfasalazine
Generic Name
sulfasalazine
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
sulfasalazine 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-6936
Product ID
50090-6936_21baf22f-e456-4e4b-a46b-2c354e255ba0
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA007073
Listing Expiration
2026-12-31
Marketing Start
2003-07-01
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500906936
Hyphenated Format
50090-6936
Supplemental Identifiers
RxCUI
UNII
NUI
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
sulfasalazine (source: ndc)
Generic Name
sulfasalazine (source: ndc)
Application Number
NDA007073 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 90 TABLET in 1 BOTTLE (50090-6936-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "21baf22f-e456-4e4b-a46b-2c354e255ba0", "openfda": {"nui": ["N0000175781", "M0000971"], "unii": ["3XC8GUZ6CB"], "rxcui": ["198232"], "spl_set_id": ["76b532a3-e7ca-4929-8c51-c0f66e0806a8"], "pharm_class_cs": ["Aminosalicylic Acids [CS]"], "pharm_class_epc": ["Aminosalicylate [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6936-0)", "package_ndc": "50090-6936-0", "marketing_start_date": "20231215"}], "brand_name": "Sulfasalazine", "product_id": "50090-6936_21baf22f-e456-4e4b-a46b-2c354e255ba0", "dosage_form": "TABLET", "pharm_class": ["Aminosalicylate [EPC]", "Aminosalicylic Acids [CS]"], "product_ndc": "50090-6936", "generic_name": "Sulfasalazine", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sulfasalazine", "active_ingredients": [{"name": "SULFASALAZINE", "strength": "500 mg/1"}], "application_number": "NDA007073", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20030701", "listing_expiration_date": "20261231"}