Package 90096-161-01

Brand: naproxen

Generic: naproxen
NDC Package

Package Facts

Identity

Package NDC 90096-161-01
Digits Only 9009616101
Product NDC 90096-161
Description

100 TABLET, DELAYED RELEASE in 1 BOTTLE (90096-161-01)

Marketing

Marketing Status
Marketed Since 2025-08-31
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": "1e574b03-a038-453b-b84f-9437fc2df0f8", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["57Y76R9ATQ"], "rxcui": ["311915"], "spl_set_id": ["d2e5553a-7c90-407c-9f07-3be65560c23a"], "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": ["Zameer Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE (90096-161-01)", "package_ndc": "90096-161-01", "marketing_start_date": "20250831"}], "brand_name": "Naproxen", "product_id": "90096-161_1e574b03-a038-453b-b84f-9437fc2df0f8", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "90096-161", "generic_name": "Naproxen", "labeler_name": "Zameer Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Naproxen", "active_ingredients": [{"name": "NAPROXEN", "strength": "500 mg/1"}], "application_number": "NDA020067", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20250831", "listing_expiration_date": "20261231"}