Package 11673-368-71

Brand: up and up naproxen sodium

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 11673-368-71
Digits Only 1167336871
Product NDC 11673-368
Product ID 11673-368_25a249be-b52a-4d7e-8352-8e6d30f3664f
Description

1 BOTTLE in 1 CARTON (11673-368-71) / 50 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2009-07-14
Brand up and up naproxen sodium
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

up and up naproxen sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "25a249be-b52a-4d7e-8352-8e6d30f3664f", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["00bd8490-f280-4336-b13d-0e11c0bf4586"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-368-71)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "11673-368-71", "marketing_start_date": "20090714"}], "brand_name": "up and up naproxen sodium", "product_id": "11673-368_25a249be-b52a-4d7e-8352-8e6d30f3664f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "11673-368", "generic_name": "Naproxen Sodium", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "up and up naproxen sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA074661", "marketing_category": "ANDA", "marketing_start_date": "20090624", "listing_expiration_date": "20261231"}