naproxen

Generic: naproxen

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

Drug Facts

Product Profile

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

naproxen 250 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0217
Product ID 71335-0217_fb26cc76-51bd-49de-9161-c8489d7a1c2c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078250
Listing Expiration 2026-12-31
Marketing Start 2007-07-01

Pharmacologic Class

Established (EPC)
nonsteroidal anti-inflammatory drug [epc]
Mechanism of Action
cyclooxygenase inhibitors [moa]
Chemical Structure
anti-inflammatory agents, non-steroidal [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713350217
Hyphenated Format 71335-0217

Supplemental Identifiers

RxCUI
198013
UNII
57Y76R9ATQ
NUI
N0000000160 M0001335 N0000175722

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 (source: ndc)
Application Number ANDA078250 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-0217-1)
  • 60 TABLET in 1 BOTTLE (71335-0217-2)
  • 20 TABLET in 1 BOTTLE (71335-0217-3)
  • 120 TABLET in 1 BOTTLE (71335-0217-4)
  • 10 TABLET in 1 BOTTLE (71335-0217-5)
  • 90 TABLET in 1 BOTTLE (71335-0217-6)
  • 40 TABLET in 1 BOTTLE (71335-0217-7)
  • 45 TABLET in 1 BOTTLE (71335-0217-8)
source: ndc

Packages (8)

71335-0217-1 30 TABLET in 1 BOTTLE (71335-0217-1) 71335-0217-2 60 TABLET in 1 BOTTLE (71335-0217-2) 71335-0217-3 20 TABLET in 1 BOTTLE (71335-0217-3) 71335-0217-4 120 TABLET in 1 BOTTLE (71335-0217-4) 71335-0217-5 10 TABLET in 1 BOTTLE (71335-0217-5) 71335-0217-6 90 TABLET in 1 BOTTLE (71335-0217-6) 71335-0217-7 40 TABLET in 1 BOTTLE (71335-0217-7) 71335-0217-8 45 TABLET in 1 BOTTLE (71335-0217-8)

Ingredients (1)

naproxen (250 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": "fb26cc76-51bd-49de-9161-c8489d7a1c2c", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["57Y76R9ATQ"], "rxcui": ["198013"], "spl_set_id": ["da61463f-f87b-4aba-b538-7264252cadb8"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0217-1)", "package_ndc": "71335-0217-1", "marketing_start_date": "20180420"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0217-2)", "package_ndc": "71335-0217-2", "marketing_start_date": "20180215"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-0217-3)", "package_ndc": "71335-0217-3", "marketing_start_date": "20240905"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-0217-4)", "package_ndc": "71335-0217-4", "marketing_start_date": "20240905"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-0217-5)", "package_ndc": "71335-0217-5", "marketing_start_date": "20240905"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0217-6)", "package_ndc": "71335-0217-6", "marketing_start_date": "20240905"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (71335-0217-7)", "package_ndc": "71335-0217-7", "marketing_start_date": "20240905"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (71335-0217-8)", "package_ndc": "71335-0217-8", "marketing_start_date": "20240905"}], "brand_name": "Naproxen", "product_id": "71335-0217_fb26cc76-51bd-49de-9161-c8489d7a1c2c", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "71335-0217", "generic_name": "Naproxen", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naproxen", "active_ingredients": [{"name": "NAPROXEN", "strength": "250 mg/1"}], "application_number": "ANDA078250", "marketing_category": "ANDA", "marketing_start_date": "20070701", "listing_expiration_date": "20261231"}