naproxen
Generic: naproxen
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
naproxen
Generic Name
naproxen
Labeler
american health packaging
Dosage Form
TABLET
Routes
Active Ingredients
naproxen 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
60687-491
Product ID
60687-491_3fa429c2-7507-3d5d-e063-6294a90a83af
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078250
Listing Expiration
2026-12-31
Marketing Start
2020-02-18
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60687491
Hyphenated Format
60687-491
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
ANDA078250 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-491-01) / 1 TABLET in 1 BLISTER PACK (60687-491-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3fa429c2-7507-3d5d-e063-6294a90a83af", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["57Y76R9ATQ"], "rxcui": ["198014"], "spl_set_id": ["86a3e612-3bfe-432f-9afd-972bb8a6644e"], "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": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-491-01) / 1 TABLET in 1 BLISTER PACK (60687-491-11)", "package_ndc": "60687-491-01", "marketing_start_date": "20200218"}], "brand_name": "Naproxen", "product_id": "60687-491_3fa429c2-7507-3d5d-e063-6294a90a83af", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "60687-491", "generic_name": "Naproxen", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naproxen", "active_ingredients": [{"name": "NAPROXEN", "strength": "500 mg/1"}], "application_number": "ANDA078250", "marketing_category": "ANDA", "marketing_start_date": "20200218", "listing_expiration_date": "20261231"}