sulindac

Generic: sulindac

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sulindac
Generic Name sulindac
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

sulindac 200 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-648
Product ID 71205-648_d94e8865-d151-4fb1-bacd-f4e43819e3c2
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)
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 71205648
Hyphenated Format 71205-648

Supplemental Identifiers

RxCUI
198239
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 ANDA072711 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71205-648-30)
  • 60 TABLET in 1 BOTTLE (71205-648-60)
  • 90 TABLET in 1 BOTTLE (71205-648-90)
source: ndc

Packages (3)

71205-648-30 30 TABLET in 1 BOTTLE (71205-648-30) 71205-648-60 60 TABLET in 1 BOTTLE (71205-648-60) 71205-648-90 90 TABLET in 1 BOTTLE (71205-648-90)

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": "d94e8865-d151-4fb1-bacd-f4e43819e3c2", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["184SNS8VUH"], "rxcui": ["198239"], "spl_set_id": ["d94e8865-d151-4fb1-bacd-f4e43819e3c2"], "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": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-648-30)", "package_ndc": "71205-648-30", "marketing_start_date": "20220328"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-648-60)", "package_ndc": "71205-648-60", "marketing_start_date": "20220328"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-648-90)", "package_ndc": "71205-648-90", "marketing_start_date": "20220328"}], "brand_name": "SULINDAC", "product_id": "71205-648_d94e8865-d151-4fb1-bacd-f4e43819e3c2", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "71205-648", "generic_name": "SULINDAC", "labeler_name": "Proficient Rx LP", "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"}