sulindac

Generic: sulindac

Labeler: epic pharma, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sulindac
Generic Name sulindac
Labeler epic pharma, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sulindac 150 mg/1

Manufacturer
Epic Pharma, LLC

Identifiers & Regulatory

Product NDC 42806-018
Product ID 42806-018_fb793a0a-affa-4f9a-a5b4-aa1c84aa475e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA072710
Listing Expiration 2026-12-31
Marketing Start 2010-01-25

Pharmacologic Class

Established (EPC)
nonsteroidal anti-inflammatory drug [epc]
Mechanism of Action
cyclooxygenase inhibitors [moa]
Chemical Structure
anti-inflammatory agents, non-steroidal [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42806018
Hyphenated Format 42806-018

Supplemental Identifiers

RxCUI
198238 198239
UPC
0342806018057 0342806011010
UNII
184SNS8VUH
NUI
N0000000160 M0001335 N0000175722

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 sulindac (source: ndc)
Generic Name sulindac (source: ndc)
Application Number ANDA072710 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (42806-018-01)
  • 500 TABLET in 1 BOTTLE (42806-018-05)
  • 1000 TABLET in 1 BOTTLE (42806-018-10)
source: ndc

Packages (3)

Ingredients (1)

sulindac (150 mg/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 (42806-018-01)", "package_ndc": "42806-018-01", "marketing_start_date": "20100125"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (42806-018-05)", "package_ndc": "42806-018-05", "marketing_start_date": "20100125"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (42806-018-10)", "package_ndc": "42806-018-10", "marketing_start_date": "20100125"}], "brand_name": "SULINDAC", "product_id": "42806-018_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": "42806-018", "generic_name": "SULINDAC", "labeler_name": "Epic Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SULINDAC", "active_ingredients": [{"name": "SULINDAC", "strength": "150 mg/1"}], "application_number": "ANDA072710", "marketing_category": "ANDA", "marketing_start_date": "20100125", "listing_expiration_date": "20261231"}