Package 50844-714-14
Brand: naproxen back and muscle pain
Generic: naproxen sodiumPackage Facts
Identity
Package NDC
50844-714-14
Digits Only
5084471414
Product NDC
50844-714
Description
500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-14)
Marketing
Marketing Status
Brand
naproxen back and muscle pain
Generic
naproxen sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "bc397444-6e0e-4b4e-8f03-d6372588d8ab", "openfda": {"upc": ["0350844714169"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["68944663-0dc0-4d3a-a36b-019061bdbfa0"], "manufacturer_name": ["L.N.K. International, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-14)", "package_ndc": "50844-714-14", "marketing_start_date": "20190201"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-16)", "package_ndc": "50844-714-16", "marketing_start_date": "20190201"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (50844-714-19) / 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "50844-714-19", "marketing_start_date": "20190201"}, {"sample": false, "description": "25 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-56)", "package_ndc": "50844-714-56", "marketing_start_date": "20190201"}, {"sample": false, "description": "8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-98)", "package_ndc": "50844-714-98", "marketing_start_date": "20190201"}, {"sample": false, "description": "8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-99)", "package_ndc": "50844-714-99", "marketing_start_date": "20190201"}], "brand_name": "Naproxen Back and Muscle Pain", "product_id": "50844-714_bc397444-6e0e-4b4e-8f03-d6372588d8ab", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "50844-714", "generic_name": "Naproxen Sodium", "labeler_name": "L.N.K. International, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Back and Muscle Pain", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA204872", "marketing_category": "ANDA", "marketing_start_date": "20190201", "listing_expiration_date": "20271231"}