medique at home mediproxen
Generic: naproxen sodium
Labeler: unifirst first aid corporationDrug Facts
Product Profile
Brand Name
medique at home mediproxen
Generic Name
naproxen sodium
Labeler
unifirst first aid corporation
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
naproxen sodium 220 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
47682-737
Product ID
47682-737_3e5d544f-38be-42a3-e063-6294a90aebbf
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA079096
Listing Expiration
2026-12-31
Marketing Start
2021-02-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
47682737
Hyphenated Format
47682-737
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
medique at home mediproxen (source: ndc)
Generic Name
naproxen sodium (source: ndc)
Application Number
ANDA079096 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 220 mg/1
Packaging
- 50 PACKET in 1 BOX (47682-737-50) / 1 TABLET, FILM COATED in 1 PACKET (47682-737-46)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3e5d544f-38be-42a3-e063-6294a90aebbf", "openfda": {"upc": ["0347682737504"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["b591ba4f-d7d3-4c81-e053-2995a90a7c6e"], "manufacturer_name": ["Unifirst First Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 PACKET in 1 BOX (47682-737-50) / 1 TABLET, FILM COATED in 1 PACKET (47682-737-46)", "package_ndc": "47682-737-50", "marketing_start_date": "20210201"}], "brand_name": "Medique at Home Mediproxen", "product_id": "47682-737_3e5d544f-38be-42a3-e063-6294a90aebbf", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "47682-737", "generic_name": "Naproxen Sodium", "labeler_name": "Unifirst First Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Medique at Home Mediproxen", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA079096", "marketing_category": "ANDA", "marketing_start_date": "20210201", "listing_expiration_date": "20261231"}