Package 68391-368-79

Brand: berkley and jensen naproxen sodium

Generic: naproxen sodium
NDC Package

Package Facts

Identity

Package NDC 68391-368-79
Digits Only 6839136879
Product NDC 68391-368
Product ID 68391-368_1d371cd3-2938-4ed8-b820-ec37c1017045
Description

400 TABLET, FILM COATED in 1 BOTTLE (68391-368-79)

Marketing

Marketing Status
Marketed Since 2011-04-15
Brand berkley and jensen naproxen sodium
Generic naproxen sodium
Sample Package No

Linked Drug Pages (1)

Berkley and Jensen Naproxen Sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1d371cd3-2938-4ed8-b820-ec37c1017045", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["9530b649-3e01-452c-99a6-cff47fa4085b"], "manufacturer_name": ["BJWC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "400 TABLET, FILM COATED in 1 BOTTLE (68391-368-79)", "package_ndc": "68391-368-79", "marketing_start_date": "20110415"}], "brand_name": "Berkley and Jensen Naproxen Sodium", "product_id": "68391-368_1d371cd3-2938-4ed8-b820-ec37c1017045", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68391-368", "generic_name": "Naproxen Sodium", "labeler_name": "BJWC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Berkley and Jensen Naproxen Sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA074661", "marketing_category": "ANDA", "marketing_start_date": "20070917", "listing_expiration_date": "20261231"}