nalfon

Generic: fenoprofen calcium

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

Drug Facts

Product Profile

Brand Name nalfon
Generic Name fenoprofen calcium
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

fenoprofen calcium 600 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-129
Product ID 82804-129_01f6c461-8144-4de1-88e1-bc56defd08f3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA072267
Listing Expiration 2026-12-31
Marketing Start 2018-09-24

Pharmacologic Class

Classes
anti-inflammatory agents non-steroidal [cs] cyclooxygenase inhibitors [moa] nonsteroidal anti-inflammatory drug [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82804129
Hyphenated Format 82804-129

Supplemental Identifiers

RxCUI
310291 351398
UPC
0382804129904
UNII
0X2CW1QABJ

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 nalfon (source: ndc)
Generic Name fenoprofen calcium (source: ndc)
Application Number ANDA072267 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 90 TABLET, FILM COATED in 1 BOTTLE (82804-129-90)
source: ndc

Packages (1)

82804-129-90 90 TABLET, FILM COATED in 1 BOTTLE (82804-129-90)

Ingredients (1)

fenoprofen calcium (600 mg/1)

Linked Drug Pages (1)

NALFON ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "01f6c461-8144-4de1-88e1-bc56defd08f3", "openfda": {"upc": ["0382804129904"], "unii": ["0X2CW1QABJ"], "rxcui": ["310291", "351398"], "spl_set_id": ["01f6c461-8144-4de1-88e1-bc56defd08f3"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (82804-129-90)", "package_ndc": "82804-129-90", "marketing_start_date": "20240723"}], "brand_name": "NALFON", "product_id": "82804-129_01f6c461-8144-4de1-88e1-bc56defd08f3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "82804-129", "generic_name": "Fenoprofen Calcium", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NALFON", "active_ingredients": [{"name": "FENOPROFEN CALCIUM", "strength": "600 mg/1"}], "application_number": "ANDA072267", "marketing_category": "ANDA", "marketing_start_date": "20180924", "listing_expiration_date": "20261231"}