Package 68071-5039-1

Brand: naproxen

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 68071-5039-1
Digits Only 6807150391
Product NDC 68071-5039
Product ID 68071-5039_2d53b71b-770a-e12d-e063-6294a90a5478
Description

21 TABLET in 1 BOTTLE (68071-5039-1)

Marketing

Marketing Status
Marketed Since 2023-01-10
Brand naproxen
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

Naproxen ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2d53b71b-770a-e12d-e063-6294a90a5478", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["f1ed8384-83d6-6f2a-e053-2a95a90ab08f"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 BOTTLE (68071-5039-1)", "package_ndc": "68071-5039-1", "marketing_start_date": "20230110"}], "brand_name": "Naproxen", "product_id": "68071-5039_2d53b71b-770a-e12d-e063-6294a90a5478", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68071-5039", "generic_name": "Naproxen Sodium", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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"}