Package 72189-136-20

Brand: naproxen

Generic: naproxen
NDC Package

Package Facts

Identity

Package NDC 72189-136-20
Digits Only 7218913620
Product NDC 72189-136
Description

20 TABLET in 1 BOTTLE (72189-136-20)

Marketing

Marketing Status
Marketed Since 2020-10-15
Brand naproxen
Generic naproxen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2be91642-ea9b-b147-e063-6394a90a2d96", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["57Y76R9ATQ"], "rxcui": ["198014"], "spl_set_id": ["b1b78c49-82e9-2402-e053-2a95a90ae35f"], "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": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET in 1 BOTTLE (72189-136-14)", "package_ndc": "72189-136-14", "marketing_start_date": "20201015"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (72189-136-20)", "package_ndc": "72189-136-20", "marketing_start_date": "20201015"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-136-30)", "package_ndc": "72189-136-30", "marketing_start_date": "20201015"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (72189-136-60)", "package_ndc": "72189-136-60", "marketing_start_date": "20201015"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (72189-136-71)", "package_ndc": "72189-136-71", "marketing_start_date": "20201015"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-136-90)", "package_ndc": "72189-136-90", "marketing_start_date": "20201015"}], "brand_name": "NAPROXEN", "product_id": "72189-136_2be91642-ea9b-b147-e063-6394a90a2d96", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "72189-136", "generic_name": "NAPROXEN", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NAPROXEN", "active_ingredients": [{"name": "NAPROXEN", "strength": "500 mg/1"}], "application_number": "ANDA091416", "marketing_category": "ANDA", "marketing_start_date": "20201015", "listing_expiration_date": "20261231"}