flanax pain reliever/fever reducer

Generic: naproxen sodium

Labeler: navajo manufacturing company inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name flanax pain reliever/fever reducer
Generic Name naproxen sodium
Labeler navajo manufacturing company inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

naproxen sodium 220 mg/1

Manufacturer
Navajo Manufacturing Company Inc.

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
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 67751125
Hyphenated Format 67751-125

Supplemental Identifiers

RxCUI
849574
UNII
9TN87S3A3C

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 220 mg/1
source: ndc
Packaging
  • 1 PACKET in 1 CARTON (67751-125-01) / 2 TABLET in 1 PACKET
source: ndc

Packages (1)

Ingredients (1)

naproxen sodium (220 mg/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"}