naproxen sodium
Generic: naproxen sodium
Labeler: marc glassman, inc.Drug Facts
Product Profile
Brand Name
naproxen sodium
Generic Name
naproxen sodium
Labeler
marc glassman, inc.
Dosage Form
TABLET, COATED
Routes
Active Ingredients
naproxen sodium 220 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68998-144
Product ID
68998-144_39f8149e-965d-b6b6-e063-6294a90a8f9a
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA079096
Listing Expiration
2026-12-31
Marketing Start
2009-06-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68998144
Hyphenated Format
68998-144
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 (source: ndc)
Generic Name
naproxen sodium (source: ndc)
Application Number
ANDA079096 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 220 mg/1
Packaging
- 1 BOTTLE, PLASTIC in 1 CARTON (68998-144-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "39f8149e-965d-b6b6-e063-6294a90a8f9a", "openfda": {"upc": ["0099581910822"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["684e03b6-74eb-4374-a512-1c01ea216b51"], "manufacturer_name": ["Marc Glassman, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68998-144-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC", "package_ndc": "68998-144-03", "marketing_start_date": "20090601"}], "brand_name": "Naproxen Sodium", "product_id": "68998-144_39f8149e-965d-b6b6-e063-6294a90a8f9a", "dosage_form": "TABLET, COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68998-144", "generic_name": "NAPROXEN SODIUM", "labeler_name": "Marc Glassman, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA079096", "marketing_category": "ANDA", "marketing_start_date": "20090601", "listing_expiration_date": "20261231"}