flurbiprofen

Generic: flurbiprofen

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name flurbiprofen
Generic Name flurbiprofen
Labeler nucare pharmaceuticals,inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

flurbiprofen 100 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-4436
Product ID 68071-4436_1a8c403f-badb-36b1-e063-6394a90a18d5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074431
Listing Expiration 2026-12-31
Marketing Start 1995-06-02

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 680714436
Hyphenated Format 68071-4436

Supplemental Identifiers

RxCUI
197724
UPC
0368071443646
UNII
5GRO578KLP
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 flurbiprofen (source: ndc)
Generic Name flurbiprofen (source: ndc)
Application Number ANDA074431 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 14 TABLET, FILM COATED in 1 BOTTLE (68071-4436-4)
source: ndc

Packages (1)

Ingredients (1)

flurbiprofen (100 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1a8c403f-badb-36b1-e063-6394a90a18d5", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0368071443646"], "unii": ["5GRO578KLP"], "rxcui": ["197724"], "spl_set_id": ["6c6a0daa-de1b-5455-e053-2991aa0a4cf8"], "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": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (68071-4436-4)", "package_ndc": "68071-4436-4", "marketing_start_date": "20180517"}], "brand_name": "Flurbiprofen", "product_id": "68071-4436_1a8c403f-badb-36b1-e063-6394a90a18d5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68071-4436", "generic_name": "Flurbiprofen", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Flurbiprofen", "active_ingredients": [{"name": "FLURBIPROFEN", "strength": "100 mg/1"}], "application_number": "ANDA074431", "marketing_category": "ANDA", "marketing_start_date": "19950602", "listing_expiration_date": "20261231"}