medique mediproxen

Generic: naproxen sodium

Labeler: unifirst first aid corporation
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name medique mediproxen
Generic Name naproxen sodium
Labeler unifirst first aid corporation
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

naproxen sodium 220 mg/1

Manufacturer
Unifirst First Aid Corporation

Identifiers & Regulatory

Product NDC 47682-237
Product ID 47682-237_3e4cf134-89dd-0093-e063-6394a90a3c63
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA079096
Listing Expiration 2026-12-31
Marketing Start 2008-12-30

Pharmacologic Class

Classes
anti-inflammatory agents non-steroidal [cs] cyclooxygenase inhibitors [moa] nonsteroidal anti-inflammatory drug [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 47682237
Hyphenated Format 47682-237

Supplemental Identifiers

RxCUI
849574
UNII
9TN87S3A3C

Packaging Origin

Original Packager
true

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 mediproxen (source: ndc)
Generic Name naproxen sodium (source: ndc)
Application Number ANDA079096 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 220 mg/1
source: ndc
Packaging
  • 100 PACKET in 1 BOX (47682-237-33) / 1 TABLET, FILM COATED in 1 PACKET (47682-237-46)
  • 1 TABLET, FILM COATED in 1 PACKET (47682-237-46)
  • 50 PACKET in 1 BOX (47682-237-50) / 1 TABLET, FILM COATED in 1 PACKET
source: ndc

Packages (3)

47682-237-33 100 PACKET in 1 BOX (47682-237-33) / 1 TABLET, FILM COATED in 1 PACKET (47682-237-46) 47682-237-46 1 TABLET, FILM COATED in 1 PACKET (47682-237-46) 47682-237-50 50 PACKET in 1 BOX (47682-237-50) / 1 TABLET, FILM COATED in 1 PACKET

Ingredients (1)

naproxen sodium (220 mg/1)

Linked Drug Pages (1)

Medique Mediproxen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3e4cf134-89dd-0093-e063-6394a90a3c63", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["f6261d45-df1f-483b-b013-3cd6f78d9d43"], "manufacturer_name": ["Unifirst First Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 PACKET in 1 BOX (47682-237-33)  / 1 TABLET, FILM COATED in 1 PACKET (47682-237-46)", "package_ndc": "47682-237-33", "marketing_start_date": "20081230"}, {"sample": false, "description": "1 TABLET, FILM COATED in 1 PACKET (47682-237-46)", "package_ndc": "47682-237-46", "marketing_start_date": "20081230"}, {"sample": false, "description": "50 PACKET in 1 BOX (47682-237-50)  / 1 TABLET, FILM COATED in 1 PACKET", "package_ndc": "47682-237-50", "marketing_start_date": "20081230"}], "brand_name": "Medique Mediproxen", "product_id": "47682-237_3e4cf134-89dd-0093-e063-6394a90a3c63", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "47682-237", "generic_name": "NAPROXEN SODIUM", "labeler_name": "Unifirst First Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Medique Mediproxen", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA079096", "marketing_category": "ANDA", "marketing_start_date": "20081230", "listing_expiration_date": "20261231"}