Package 62207-814-38

{"route": ["ORAL"], "spl_id": "3b4ca636-ecbd-6807-e063-6294a90a7765", "openfda": {"unii": ["TC2D6JAD40", "9TN87S3A3C"], "rxcui": ["1550957"], "spl_set_id": ["0d59780a-ef22-4b67-8b42-9795dbec8db0"], "manufacturer_name": ["Granules India Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "37500 TABLET, FILM COATED in 1 POUCH (62207-814-38)", "package_ndc": "62207-814-38", "marketing_start_date": "20210220"}, {"sample": false, "description": "7500 TABLET, FILM COATED in 1 POUCH (62207-814-39)", "package_ndc": "62207-814-39", "marketing_start_date": "20210220"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (62207-814-47)", "package_ndc": "62207-814-47", "marketing_start_date": "20210220"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (62207-814-95)  / 20 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "62207-814-95", "marketing_start_date": "20210220"}], "brand_name": "Naproxen Sodium and Diphenhydramine HCl", "product_id": "62207-814_3b4ca636-ecbd-6807-e063-6294a90a7765", "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": "62207-814", "generic_name": "Naproxen Sodium and Diphenhydramine HCl", "labeler_name": "Granules India Ltd", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naproxen Sodium and 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": "20210220", "listing_expiration_date": "20261231"}