sulindac

Generic: sulindac

Labeler: puracap laboratories llc dba blu pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sulindac
Generic Name sulindac
Labeler puracap laboratories llc dba blu pharmaceuticals
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sulindac 200 mg/1

Manufacturer
PuraCap Laboratories LLC dba Blu Pharmaceuticals

Identifiers & Regulatory

Product NDC 24658-771
Product ID 24658-771_cb28dfa2-28af-47a2-ab7f-1c65720d9496
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA072711
Listing Expiration 2026-12-31
Marketing Start 2016-11-14

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 24658771
Hyphenated Format 24658-771

Supplemental Identifiers

RxCUI
198238 198239
UPC
0324658771014 0324658770055
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 ANDA072711 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (24658-771-01)
  • 500 TABLET in 1 BOTTLE (24658-771-05)
source: ndc

Packages (2)

24658-771-01 100 TABLET in 1 BOTTLE (24658-771-01) 24658-771-05 500 TABLET in 1 BOTTLE (24658-771-05)

Ingredients (1)

sulindac (200 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": "cb28dfa2-28af-47a2-ab7f-1c65720d9496", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0324658771014", "0324658770055"], "unii": ["184SNS8VUH"], "rxcui": ["198238", "198239"], "spl_set_id": ["0feabf47-8d0d-48c0-b263-43db4969f39e"], "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": ["PuraCap Laboratories LLC dba Blu Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (24658-771-01)", "package_ndc": "24658-771-01", "marketing_start_date": "20161114"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (24658-771-05)", "package_ndc": "24658-771-05", "marketing_start_date": "20161114"}], "brand_name": "SULINDAC", "product_id": "24658-771_cb28dfa2-28af-47a2-ab7f-1c65720d9496", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "24658-771", "generic_name": "SULINDAC", "labeler_name": "PuraCap Laboratories LLC dba Blu Pharmaceuticals", "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": "20161114", "listing_expiration_date": "20261231"}