naproxen

Generic: naproxen sodium

Labeler: bryant ranch prepack
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name naproxen
Generic Name naproxen sodium
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

naproxen sodium 220 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1282
Product ID 71335-1282_1245c4fb-1cb1-42f8-962d-f059c222ed3f
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 713351282
Hyphenated Format 71335-1282

Supplemental Identifiers

RxCUI
849574
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
  • 20 TABLET in 1 BOTTLE (71335-1282-1)
  • 30 TABLET in 1 BOTTLE (71335-1282-2)
  • 40 TABLET in 1 BOTTLE (71335-1282-3)
  • 50 TABLET in 1 BOTTLE (71335-1282-4)
  • 60 TABLET in 1 BOTTLE (71335-1282-5)
  • 14 TABLET in 1 BOTTLE (71335-1282-6)
  • 100 TABLET in 1 BOTTLE (71335-1282-7)
  • 90 TABLET in 1 BOTTLE (71335-1282-8)
  • 24 TABLET in 1 BOTTLE (71335-1282-9)
source: ndc

Packages (9)

71335-1282-1 20 TABLET in 1 BOTTLE (71335-1282-1) 71335-1282-2 30 TABLET in 1 BOTTLE (71335-1282-2) 71335-1282-3 40 TABLET in 1 BOTTLE (71335-1282-3) 71335-1282-4 50 TABLET in 1 BOTTLE (71335-1282-4) 71335-1282-5 60 TABLET in 1 BOTTLE (71335-1282-5) 71335-1282-6 14 TABLET in 1 BOTTLE (71335-1282-6) 71335-1282-7 100 TABLET in 1 BOTTLE (71335-1282-7) 71335-1282-8 90 TABLET in 1 BOTTLE (71335-1282-8) 71335-1282-9 24 TABLET in 1 BOTTLE (71335-1282-9)

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": "1245c4fb-1cb1-42f8-962d-f059c222ed3f", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["f9ddc614-26b7-48dc-ae93-02da6388f2d5"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-1282-1)", "package_ndc": "71335-1282-1", "marketing_start_date": "20211118"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1282-2)", "package_ndc": "71335-1282-2", "marketing_start_date": "20190827"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (71335-1282-3)", "package_ndc": "71335-1282-3", "marketing_start_date": "20191022"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (71335-1282-4)", "package_ndc": "71335-1282-4", "marketing_start_date": "20250110"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1282-5)", "package_ndc": "71335-1282-5", "marketing_start_date": "20250130"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (71335-1282-6)", "package_ndc": "71335-1282-6", "marketing_start_date": "20191126"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-1282-7)", "package_ndc": "71335-1282-7", "marketing_start_date": "20191025"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1282-8)", "package_ndc": "71335-1282-8", "marketing_start_date": "20250130"}, {"sample": false, "description": "24 TABLET in 1 BOTTLE (71335-1282-9)", "package_ndc": "71335-1282-9", "marketing_start_date": "20250130"}], "brand_name": "Naproxen", "product_id": "71335-1282_1245c4fb-1cb1-42f8-962d-f059c222ed3f", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "71335-1282", "generic_name": "Naproxen Sodium", "labeler_name": "Bryant Ranch Prepack", "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"}