Package 51316-762-70

Brand: naproxen sodium

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 51316-762-70
Digits Only 5131676270
Product NDC 51316-762
Product ID 51316-762_4654533f-58ca-750a-e063-6294a90a2783
Description

270 TABLET in 1 BOTTLE (51316-762-70)

Marketing

Marketing Status
Marketed Since 2024-05-25
Brand naproxen sodium
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

Naproxen Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4654533f-58ca-750a-e063-6294a90a2783", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["1042b202-e8ee-1839-e063-6294a90ac90b"], "manufacturer_name": ["CVS"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "270 TABLET in 1 BOTTLE (51316-762-70)", "package_ndc": "51316-762-70", "marketing_start_date": "20240525"}], "brand_name": "Naproxen Sodium", "product_id": "51316-762_4654533f-58ca-750a-e063-6294a90a2783", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "51316-762", "generic_name": "Naproxen Sodium", "labeler_name": "CVS", "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": "20240525", "listing_expiration_date": "20261231"}