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 200 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 55289-930
Product ID 55289-930_30ca698c-7fb2-9fa7-e063-6294a90abd86
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071795
Listing Expiration 2026-12-31
Marketing Start 1990-04-03

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 55289930
Hyphenated Format 55289-930

Supplemental Identifiers

RxCUI
198239
UPC
0355289930105
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 ANDA071795 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10)
  • 20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20)
  • 30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30)
source: ndc

Packages (3)

Ingredients (1)

sulindac (200 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "30ca698c-7fb2-9fa7-e063-6294a90abd86", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0355289930105"], "unii": ["184SNS8VUH"], "rxcui": ["198239"], "spl_set_id": ["68d4eeed-2501-494b-b979-502720de86c0"], "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": "10 TABLET in 1 BOTTLE, PLASTIC (55289-930-10)", "package_ndc": "55289-930-10", "marketing_start_date": "20100712"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE, PLASTIC (55289-930-20)", "package_ndc": "55289-930-20", "marketing_start_date": "20100712"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (55289-930-30)", "package_ndc": "55289-930-30", "marketing_start_date": "20100712"}], "brand_name": "Sulindac", "product_id": "55289-930_30ca698c-7fb2-9fa7-e063-6294a90abd86", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "55289-930", "generic_name": "Sulindac", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sulindac", "active_ingredients": [{"name": "SULINDAC", "strength": "200 mg/1"}], "application_number": "ANDA071795", "marketing_category": "ANDA", "marketing_start_date": "19900403", "listing_expiration_date": "20261231"}