Package 71141-182-32
Brand: naproxen sodium
Generic: naproxen sodiumPackage Facts
Identity
Package NDC
71141-182-32
Digits Only
7114118232
Product NDC
71141-182
Description
1 BOTTLE, PLASTIC in 1 CARTON (71141-182-32) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
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": "5018f0ff-a5e0-4086-899d-bf0f4edaf251", "openfda": {"upc": ["4056489731825"], "unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["3d01220c-c5ec-4604-8cef-9ecb807ccd53"], "manufacturer_name": ["Lidl US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (71141-182-32) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "71141-182-32", "marketing_start_date": "20230522"}], "brand_name": "Naproxen Sodium", "product_id": "71141-182_5018f0ff-a5e0-4086-899d-bf0f4edaf251", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "71141-182", "generic_name": "Naproxen Sodium", "labeler_name": "Lidl US LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA204872", "marketing_category": "ANDA", "marketing_start_date": "20230522", "listing_expiration_date": "20261231"}