naproxen

Generic: naproxen sodium

Labeler: proficient rx lp
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name naproxen
Generic Name naproxen sodium
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

naproxen sodium 220 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-595
Product ID 71205-595_0193d608-f4a8-5a69-e063-6294a90aafe8
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA204872
Listing Expiration 2026-12-31
Marketing Start 2019-01-01

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 71205595
Hyphenated Format 71205-595

Supplemental Identifiers

RxCUI
849574
UPC
0371205595241
UNII
9TN87S3A3C

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 (source: ndc)
Generic Name naproxen sodium (source: ndc)
Application Number ANDA204872 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 220 mg/1
source: ndc
Packaging
  • 24 TABLET in 1 BOTTLE (71205-595-24)
  • 30 TABLET in 1 BOTTLE (71205-595-30)
  • 60 TABLET in 1 BOTTLE (71205-595-60)
  • 90 TABLET in 1 BOTTLE (71205-595-90)
source: ndc

Packages (4)

71205-595-24 24 TABLET in 1 BOTTLE (71205-595-24) 71205-595-30 30 TABLET in 1 BOTTLE (71205-595-30) 71205-595-60 60 TABLET in 1 BOTTLE (71205-595-60) 71205-595-90 90 TABLET in 1 BOTTLE (71205-595-90)

Ingredients (1)

naproxen sodium (220 mg/1)

Linked Drug Pages (1)

Naproxen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0193d608-f4a8-5a69-e063-6294a90aafe8", "openfda": {"upc": ["0371205595241"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["2acd8e24-449d-4f5c-9323-504013ff4bf5"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "24 TABLET in 1 BOTTLE (71205-595-24)", "package_ndc": "71205-595-24", "marketing_start_date": "20230728"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-595-30)", "package_ndc": "71205-595-30", "marketing_start_date": "20210727"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-595-60)", "package_ndc": "71205-595-60", "marketing_start_date": "20210727"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-595-90)", "package_ndc": "71205-595-90", "marketing_start_date": "20210727"}], "brand_name": "Naproxen", "product_id": "71205-595_0193d608-f4a8-5a69-e063-6294a90aafe8", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "71205-595", "generic_name": "Naproxen Sodium", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA204872", "marketing_category": "ANDA", "marketing_start_date": "20190101", "listing_expiration_date": "20261231"}