Package 51316-608-90
Brand: naproxen sodium
Generic: naproxen sodium 220mgPackage Facts
Identity
Package NDC
51316-608-90
Digits Only
5131660890
Product NDC
51316-608
Description
90 TABLET in 1 BOTTLE (51316-608-90)
Marketing
Marketing Status
Brand
naproxen sodium
Generic
naproxen sodium 220mg
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3c14f8af-cefb-ec0f-e063-6394a90a2caa", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["1fde52e7-7a7f-40e8-e063-6394a90a922a"], "manufacturer_name": ["CVS Pharmacy, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (51316-608-90)", "package_ndc": "51316-608-90", "marketing_start_date": "20250501"}], "brand_name": "Naproxen Sodium", "product_id": "51316-608_3c14f8af-cefb-ec0f-e063-6394a90a2caa", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "51316-608", "generic_name": "Naproxen sodium 220mg", "labeler_name": "CVS Pharmacy, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA090545", "marketing_category": "ANDA", "marketing_start_date": "20250501", "listing_expiration_date": "20261231"}