naproxen sodium 220mg
Generic: naproxen sodium
Labeler: medline industries, lpDrug Facts
Product Profile
Brand Name
naproxen sodium 220mg
Generic Name
naproxen sodium
Labeler
medline industries, lp
Dosage Form
TABLET
Routes
Active Ingredients
naproxen sodium 220 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
53329-688
Product ID
53329-688_2876e756-1812-62d6-e063-6394a90a4a0d
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA090545
Listing Expiration
2026-12-31
Marketing Start
2018-08-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
53329688
Hyphenated Format
53329-688
Supplemental Identifiers
RxCUI
UPC
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 220mg (source: ndc)
Generic Name
naproxen sodium (source: ndc)
Application Number
ANDA090545 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 220 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (53329-688-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2876e756-1812-62d6-e063-6394a90a4a0d", "openfda": {"upc": ["0888277699840"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["6d9b3581-63b5-699e-e053-2991aa0a68f8"], "manufacturer_name": ["Medline Industries, LP"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (53329-688-30)", "package_ndc": "53329-688-30", "marketing_start_date": "20180801"}], "brand_name": "Naproxen Sodium 220mg", "product_id": "53329-688_2876e756-1812-62d6-e063-6394a90a4a0d", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "53329-688", "generic_name": "Naproxen Sodium", "labeler_name": "Medline Industries, LP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium 220mg", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA090545", "marketing_category": "ANDA", "marketing_start_date": "20180801", "listing_expiration_date": "20261231"}