Package 11673-764-09

Brand: naproxen sodium

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 11673-764-09
Digits Only 1167376409
Product NDC 11673-764
Description

90 TABLET in 1 BOTTLE (11673-764-09)

Marketing

Marketing Status
Marketed Since 2024-03-01
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": "46532fbb-e0e4-8e66-e063-6394a90a2a2a", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["fdb87abd-3176-dd62-e053-6394a90a6fcc"], "manufacturer_name": ["TARGET CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 TABLET in 1 BOTTLE (11673-764-05)", "package_ndc": "11673-764-05", "marketing_start_date": "20240301"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (11673-764-09)", "package_ndc": "11673-764-09", "marketing_start_date": "20240301"}], "brand_name": "Naproxen Sodium", "product_id": "11673-764_46532fbb-e0e4-8e66-e063-6394a90a2a2a", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "11673-764", "generic_name": "Naproxen Sodium", "labeler_name": "TARGET CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA091353", "marketing_category": "ANDA", "marketing_start_date": "20240301", "listing_expiration_date": "20261231"}