rugby all day relief
Generic: naproxen sodium
Labeler: rugby laboratoriesDrug Facts
Product Profile
Brand Name
rugby all day relief
Generic Name
naproxen sodium
Labeler
rugby laboratories
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
naproxen sodium 220 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0536-1094
Product ID
0536-1094_b4e0c57c-be39-422b-ac93-bed2dc89acf7
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA074661
Listing Expiration
2026-12-31
Marketing Start
2015-09-02
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
05361094
Hyphenated Format
0536-1094
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
rugby all day relief (source: ndc)
Generic Name
naproxen sodium (source: ndc)
Application Number
ANDA074661 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 220 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (0536-1094-06) / 50 TABLET, FILM COATED in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (0536-1094-11) / 90 TABLET, FILM COATED in 1 BOTTLE
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b4e0c57c-be39-422b-ac93-bed2dc89acf7", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["f587a428-291c-4c54-80fe-244a961b0521"], "manufacturer_name": ["Rugby Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0536-1094-06) / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0536-1094-06", "marketing_start_date": "20150902"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0536-1094-11) / 90 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0536-1094-11", "marketing_start_date": "20220427"}], "brand_name": "rugby all day relief", "product_id": "0536-1094_b4e0c57c-be39-422b-ac93-bed2dc89acf7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "0536-1094", "generic_name": "Naproxen Sodium", "labeler_name": "Rugby Laboratories", "product_type": "HUMAN OTC DRUG", "brand_name_base": "rugby all day relief", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA074661", "marketing_category": "ANDA", "marketing_start_date": "20150902", "listing_expiration_date": "20261231"}