naproxen sodium
Generic: naproxen sodium
Labeler: bionpharma inc.Drug Facts
Product Profile
Brand Name
naproxen sodium
Generic Name
naproxen sodium
Labeler
bionpharma inc.
Dosage Form
CAPSULE, LIQUID FILLED
Routes
Active Ingredients
naproxen sodium 220 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
69452-179
Product ID
69452-179_0d85dc59-4954-47fc-e063-6394a90a01cd
Product Type
HUMAN OTC DRUG
Marketing Category
NDA
Application Number
NDA021920
Listing Expiration
2026-12-31
Marketing Start
2018-11-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
69452179
Hyphenated Format
69452-179
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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 sodium (source: ndc)
Generic Name
naproxen sodium (source: ndc)
Application Number
NDA021920 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 220 mg/1
Packaging
- 120 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (69452-179-22)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0d85dc59-4954-47fc-e063-6394a90a01cd", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["1112231"], "spl_set_id": ["3e10256f-0a5f-49e4-9518-a72b10490f89"], "manufacturer_name": ["Bionpharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (69452-179-22)", "package_ndc": "69452-179-22", "marketing_start_date": "20181101"}], "brand_name": "Naproxen Sodium", "product_id": "69452-179_0d85dc59-4954-47fc-e063-6394a90a01cd", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "69452-179", "generic_name": "Naproxen Sodium", "labeler_name": "Bionpharma Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "NDA021920", "marketing_category": "NDA", "marketing_start_date": "20181101", "listing_expiration_date": "20261231"}