Package 11534-211-01

Brand: naproxen

Generic: naproxen
NDC Package

Package Facts

Identity

Package NDC 11534-211-01
Digits Only 1153421101
Product NDC 11534-211
Product ID 11534-211_502c7695-7f9d-4893-b151-65111de2e2a7
Description

100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (11534-211-01)

Marketing

Marketing Status
Marketed Since 2025-12-09
Brand naproxen
Generic naproxen
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": "502c7695-7f9d-4893-b151-65111de2e2a7", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0311534212013", "0311534211016"], "unii": ["57Y76R9ATQ"], "rxcui": ["311915", "603103"], "spl_set_id": ["f2fb222a-b854-4e6f-9027-2e08aed24185"], "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": ["Sunrise Pharmaceutical, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (11534-211-01)", "package_ndc": "11534-211-01", "marketing_start_date": "20251209"}], "brand_name": "Naproxen", "product_id": "11534-211_502c7695-7f9d-4893-b151-65111de2e2a7", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "11534-211", "generic_name": "Naproxen", "labeler_name": "Sunrise Pharmaceutical, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naproxen", "active_ingredients": [{"name": "NAPROXEN", "strength": "375 mg/1"}], "application_number": "ANDA091432", "marketing_category": "ANDA", "marketing_start_date": "20251209", "listing_expiration_date": "20261231"}