Package 37808-264-60

{"route": ["ORAL"], "spl_id": "7f8e2c7c-648d-488d-bd75-b9f353ce0424", "openfda": {"unii": ["TC2D6JAD40", "9TN87S3A3C"], "rxcui": ["1550957"], "spl_set_id": ["4281faf5-7182-404f-9f53-3d9ea0354a18"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (37808-264-27)  / 80 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "37808-264-27", "marketing_start_date": "20201013"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (37808-264-60)  / 20 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "37808-264-60", "marketing_start_date": "20201013"}], "brand_name": "naproxen sodium pm", "product_id": "37808-264_7f8e2c7c-648d-488d-bd75-b9f353ce0424", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "37808-264", "generic_name": "diphenhydramine hydrochloride, naproxen sodium", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "naproxen sodium pm", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}, {"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA208499", "marketing_category": "ANDA", "marketing_start_date": "20201013", "listing_expiration_date": "20271231"}