Package 37808-652-71

{"route": ["ORAL"], "spl_id": "2892644f-e31b-4537-80b5-952a35e9d6cc", "openfda": {"unii": ["9TN87S3A3C"], "rxcui": ["849574"], "spl_set_id": ["2f9439bb-e808-4c54-ba61-f75f117c8b37"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (37808-652-62)  / 24 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "37808-652-62", "marketing_start_date": "20171114"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (37808-652-71)  / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "37808-652-71", "marketing_start_date": "20171114"}], "brand_name": "naproxen sodium", "product_id": "37808-652_2892644f-e31b-4537-80b5-952a35e9d6cc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "37808-652", "generic_name": "Naproxen Sodium", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "naproxen sodium", "active_ingredients": [{"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA074661", "marketing_category": "ANDA", "marketing_start_date": "20171114", "listing_expiration_date": "20271231"}