Package 71335-2294-1

Brand: naproxen sodium

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 71335-2294-1
Digits Only 7133522941
Product NDC 71335-2294
Product ID 71335-2294_27880452-0625-47d7-b862-3d71ea86074a
Description

500 TABLET in 1 BOTTLE (71335-2294-1)

Marketing

Marketing Status
Marketed Since 2023-12-01
Brand naproxen sodium
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

Naproxen Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "27880452-0625-47d7-b862-3d71ea86074a", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849431"], "spl_set_id": ["2794b60d-d09b-4115-9ff2-07ff15524e78"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (71335-2294-1)", "package_ndc": "71335-2294-1", "marketing_start_date": "20231201"}], "brand_name": "Naproxen Sodium", "product_id": "71335-2294_27880452-0625-47d7-b862-3d71ea86074a", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "71335-2294", "generic_name": "Naproxen Sodium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "550 mg/1"}], "application_number": "ANDA212199", "marketing_category": "ANDA", "marketing_start_date": "20191030", "listing_expiration_date": "20261231"}