sulindac
Generic: sulindac
Labeler: epic pharma, llcDrug Facts
Product Profile
Brand Name
sulindac
Generic Name
sulindac
Labeler
epic pharma, llc
Dosage Form
TABLET
Routes
Active Ingredients
sulindac 200 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
42806-011
Product ID
42806-011_fb793a0a-affa-4f9a-a5b4-aa1c84aa475e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA072711
Listing Expiration
2026-12-31
Marketing Start
2010-01-25
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
42806011
Hyphenated Format
42806-011
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
sulindac (source: ndc)
Generic Name
sulindac (source: ndc)
Application Number
ANDA072711 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (42806-011-01)
- 500 TABLET in 1 BOTTLE (42806-011-05)
- 1000 TABLET in 1 BOTTLE (42806-011-10)
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fb793a0a-affa-4f9a-a5b4-aa1c84aa475e", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0342806018057", "0342806011010"], "unii": ["184SNS8VUH"], "rxcui": ["198238", "198239"], "spl_set_id": ["96c73bd2-4577-487d-a642-bd8f91e94c3a"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Epic Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42806-011-01)", "package_ndc": "42806-011-01", "marketing_start_date": "20100125"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (42806-011-05)", "package_ndc": "42806-011-05", "marketing_start_date": "20100125"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (42806-011-10)", "package_ndc": "42806-011-10", "marketing_start_date": "20100125"}], "brand_name": "SULINDAC", "product_id": "42806-011_fb793a0a-affa-4f9a-a5b4-aa1c84aa475e", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "42806-011", "generic_name": "SULINDAC", "labeler_name": "Epic Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SULINDAC", "active_ingredients": [{"name": "SULINDAC", "strength": "200 mg/1"}], "application_number": "ANDA072711", "marketing_category": "ANDA", "marketing_start_date": "20100125", "listing_expiration_date": "20261231"}