Package 72189-332-60

Brand: naproxen sodium

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 72189-332-60
Digits Only 7218933260
Product NDC 72189-332
Description

60 TABLET in 1 BOTTLE (72189-332-60)

Marketing

Marketing Status
Marketed Since 2022-03-03
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": "2c3d902a-c32e-d343-e063-6394a90a5ff9", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849431"], "spl_set_id": ["d95279d9-6e2a-0bd6-e053-2a95a90a447d"], "manufacturer_name": ["Direct Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (72189-332-60)", "package_ndc": "72189-332-60", "marketing_start_date": "20220303"}], "brand_name": "Naproxen Sodium", "product_id": "72189-332_2c3d902a-c32e-d343-e063-6394a90a5ff9", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "72189-332", "generic_name": "Naproxen Sodium", "labeler_name": "Direct Rx", "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": "20220303", "listing_expiration_date": "20261231"}