Package 31722-808-60

{"route": ["ORAL"], "spl_id": "eabf0e61-425e-9c9f-e053-2a95a90ade8e", "openfda": {"upc": ["0331722807609", "0331722808606"], "unii": ["JY0WD0UA60"], "rxcui": ["996561", "996571"], "spl_set_id": ["910827aa-5320-446c-8f66-3f17c0ee36d9"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET in 1 BOTTLE (31722-808-02)", "package_ndc": "31722-808-02", "marketing_start_date": "20220926"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (31722-808-32)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "31722-808-32", "marketing_start_date": "20220926"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (31722-808-60)", "package_ndc": "31722-808-60", "marketing_start_date": "20220926"}], "brand_name": "memantine hydrochloride", "product_id": "31722-808_eabf0e61-425e-9c9f-e053-2a95a90ade8e", "dosage_form": "TABLET", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "31722-808", "generic_name": "memantine hydrochloride", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "memantine hydrochloride", "active_ingredients": [{"name": "MEMANTINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA204389", "marketing_category": "ANDA", "marketing_start_date": "20220926", "listing_expiration_date": "20261231"}