naproxen
Generic: naproxen
Labeler: advanced rx of tennessee, llcDrug Facts
Product Profile
Brand Name
naproxen
Generic Name
naproxen
Labeler
advanced rx of tennessee, llc
Dosage Form
TABLET
Routes
Active Ingredients
naproxen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
80425-0049
Product ID
80425-0049_2a989dd1-65cd-966d-e063-6294a90ae8ed
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA075927
Listing Expiration
2026-12-31
Marketing Start
2010-02-18
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
804250049
Hyphenated Format
80425-0049
Supplemental Identifiers
RxCUI
UNII
NUI
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
naproxen (source: ndc)
Generic Name
naproxen (source: ndc)
Application Number
ANDA075927 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 60 TABLET in 1 BOTTLE (80425-0049-1)
- 90 TABLET in 1 BOTTLE (80425-0049-2)
- 30 TABLET in 1 BOTTLE (80425-0049-3)
- 120 TABLET in 1 BOTTLE (80425-0049-4)
Packages (4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a989dd1-65cd-966d-e063-6294a90ae8ed", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["57Y76R9ATQ"], "rxcui": ["198014"], "spl_set_id": ["af9a94a8-3825-eabd-e053-2a95a90acd58"], "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": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (80425-0049-1)", "package_ndc": "80425-0049-1", "marketing_start_date": "20100218"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (80425-0049-2)", "package_ndc": "80425-0049-2", "marketing_start_date": "20100218"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (80425-0049-3)", "package_ndc": "80425-0049-3", "marketing_start_date": "20100218"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (80425-0049-4)", "package_ndc": "80425-0049-4", "marketing_start_date": "20100218"}], "brand_name": "Naproxen", "product_id": "80425-0049_2a989dd1-65cd-966d-e063-6294a90ae8ed", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "80425-0049", "generic_name": "Naproxen", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naproxen", "active_ingredients": [{"name": "NAPROXEN", "strength": "500 mg/1"}], "application_number": "ANDA075927", "marketing_category": "ANDA", "marketing_start_date": "20100218", "listing_expiration_date": "20261231"}