Package 79903-231-50
Brand: naproxen sodium
Generic: naproxen sodiumPackage Facts
Identity
Package NDC
79903-231-50
Digits Only
7990323150
Product NDC
79903-231
Description
1 BOTTLE in 1 CARTON (79903-231-50) / 50 TABLET, FILM COATED in 1 BOTTLE
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": "e3f151f3-398a-4404-adf3-e2d860c5ec31", "openfda": {"upc": ["0194346189083"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["09b52dd4-0434-237c-e063-6294a90ab9b5"], "manufacturer_name": ["WALMART INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (79903-231-50) / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "79903-231-50", "marketing_start_date": "20240214"}], "brand_name": "Naproxen Sodium", "product_id": "79903-231_e3f151f3-398a-4404-adf3-e2d860c5ec31", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "79903-231", "generic_name": "Naproxen Sodium", "labeler_name": "WALMART INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA205497", "marketing_category": "ANDA", "marketing_start_date": "20240214", "listing_expiration_date": "20261231"}