Package 63629-8516-1

Brand: naproxen sodium

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 63629-8516-1
Digits Only 6362985161
Product NDC 63629-8516
Description

500 TABLET in 1 BOTTLE (63629-8516-1)

Marketing

Marketing Status
Marketed Since 2019-10-30
Brand naproxen sodium
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "92a76ca5-8c83-4a3a-94e4-c0d9d26c366b", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849431"], "spl_set_id": ["bee7b482-8ba5-411d-90ee-de00df50d2b7"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (63629-8516-1)", "package_ndc": "63629-8516-1", "marketing_start_date": "20191030"}], "brand_name": "Naproxen Sodium", "product_id": "63629-8516_92a76ca5-8c83-4a3a-94e4-c0d9d26c366b", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "63629-8516", "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"}