flanax pain reliever/fever reducer
Generic: naproxen sodium
Labeler: navajo manufacturing company inc.Drug Facts
Product Profile
Brand Name
flanax pain reliever/fever reducer
Generic Name
naproxen sodium
Labeler
navajo manufacturing company inc.
Dosage Form
TABLET
Routes
Active Ingredients
naproxen sodium 220 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
67751-125
Product ID
67751-125_f706ab57-bb88-8e63-e053-6394a90a99c0
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA090545
Listing Expiration
2026-12-31
Marketing Start
2020-07-20
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
67751125
Hyphenated Format
67751-125
Supplemental Identifiers
RxCUI
UNII
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
flanax pain reliever/fever reducer (source: ndc)
Generic Name
naproxen sodium (source: ndc)
Application Number
ANDA090545 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 220 mg/1
Packaging
- 1 PACKET in 1 CARTON (67751-125-01) / 2 TABLET in 1 PACKET
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f706ab57-bb88-8e63-e053-6394a90a99c0", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["f706b406-58f2-9b82-e053-6394a90ab598"], "manufacturer_name": ["Navajo Manufacturing Company Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 PACKET in 1 CARTON (67751-125-01) / 2 TABLET in 1 PACKET", "package_ndc": "67751-125-01", "marketing_start_date": "20200720"}], "brand_name": "Flanax Pain Reliever/Fever Reducer", "product_id": "67751-125_f706ab57-bb88-8e63-e053-6394a90a99c0", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "67751-125", "generic_name": "Naproxen Sodium", "labeler_name": "Navajo Manufacturing Company Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Flanax Pain Reliever/Fever Reducer", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA090545", "marketing_category": "ANDA", "marketing_start_date": "20200720", "listing_expiration_date": "20261231"}