Package 79903-204-20

{"route": ["ORAL"], "spl_id": "464fe3e4-2030-838c-e063-6294a90acc3a", "openfda": {"unii": ["TC2D6JAD40", "9TN87S3A3C"], "rxcui": ["1550957"], "spl_set_id": ["fe810c0e-ab42-5a8a-e053-6394a90affe4"], "manufacturer_name": ["Walmart"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (79903-204-20)", "package_ndc": "79903-204-20", "marketing_start_date": "20231214"}], "brand_name": "Naproxen Sodium Diphenhydramine HCL", "product_id": "79903-204_464fe3e4-2030-838c-e063-6294a90acc3a", "dosage_form": "TABLET", "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": "79903-204", "generic_name": "Naproxen Sodium Diphenhydramine HCL", "labeler_name": "Walmart", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium Diphenhydramine HCL", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/1"}, {"name": "NAPROXEN SODIUM", "strength": "220 mg/1"}], "application_number": "ANDA213663", "marketing_category": "ANDA", "marketing_start_date": "20231214", "listing_expiration_date": "20271231"}