sulindac

Generic: sulindac

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sulindac
Generic Name sulindac
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sulindac 150 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-373
Product ID 72789-373_41d72ed1-2f68-852b-e063-6294a90a6401
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA072050
Listing Expiration 2026-12-31
Marketing Start 2009-09-04

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 72789373
Hyphenated Format 72789-373

Supplemental Identifiers

RxCUI
198238
UPC
0372789373829
UNII
184SNS8VUH
NUI
N0000000160 M0001335 N0000175722

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 ANDA072050 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (72789-373-01)
  • 500 TABLET in 1 BOTTLE, PLASTIC (72789-373-82)
source: ndc

Packages (2)

72789-373-01 100 TABLET in 1 BOTTLE, PLASTIC (72789-373-01) 72789-373-82 500 TABLET in 1 BOTTLE, PLASTIC (72789-373-82)

Ingredients (1)

sulindac (150 mg/1)

Linked Drug Pages (1)

SULINDAC ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "41d72ed1-2f68-852b-e063-6294a90a6401", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0372789373829"], "unii": ["184SNS8VUH"], "rxcui": ["198238"], "spl_set_id": ["eb7acb87-6565-4524-a91a-02064ea8bd1a"], "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": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72789-373-01)", "package_ndc": "72789-373-01", "marketing_start_date": "20240119"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (72789-373-82)", "package_ndc": "72789-373-82", "marketing_start_date": "20240125"}], "brand_name": "SULINDAC", "product_id": "72789-373_41d72ed1-2f68-852b-e063-6294a90a6401", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "72789-373", "generic_name": "sulindac", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SULINDAC", "active_ingredients": [{"name": "SULINDAC", "strength": "150 mg/1"}], "application_number": "ANDA072050", "marketing_category": "ANDA", "marketing_start_date": "20090904", "listing_expiration_date": "20261231"}