Package 59779-914-75
Brand: naproxen sodium
Generic: naproxen sodiumPackage Facts
Identity
Package NDC
59779-914-75
Digits Only
5977991475
Product NDC
59779-914
Description
90 TABLET, FILM COATED in 1 BOTTLE (59779-914-75)
Marketing
Marketing Status
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": "4efc4879-cae3-4f61-b205-32b62f006a66", "openfda": {"upc": ["0050428420577"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["f246ff56-23e4-4d39-9d73-7c0dd2b99fd3"], "manufacturer_name": ["CVS Pharmacy"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (59779-914-75)", "package_ndc": "59779-914-75", "marketing_start_date": "20220307"}], "brand_name": "naproxen sodium", "product_id": "59779-914_4efc4879-cae3-4f61-b205-32b62f006a66", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "59779-914", "generic_name": "Naproxen sodium", "labeler_name": "CVS Pharmacy", "product_type": "HUMAN OTC DRUG", "brand_name_base": "naproxen sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA074661", "marketing_category": "ANDA", "marketing_start_date": "20150722", "listing_expiration_date": "20261231"}