Package 33342-222-12

{"route": ["ORAL"], "spl_id": "1c695653-b7dd-40af-b5eb-a6e3ecbab14d", "openfda": {"unii": ["JY0WD0UA60"], "rxcui": ["996594", "996603", "996609", "996615"], "spl_set_id": ["62e32b0b-1eb2-424d-bfd2-d27ef27d35f3"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (33342-222-07)", "package_ndc": "33342-222-07", "marketing_start_date": "20250828"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (33342-222-12)  / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "33342-222-12", "marketing_start_date": "20250828"}], "brand_name": "Memantine hydrochloride", "product_id": "33342-222_1c695653-b7dd-40af-b5eb-a6e3ecbab14d", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["N-methyl-D-aspartate Receptor Antagonist [EPC]", "NMDA Receptor Antagonists [MoA]"], "product_ndc": "33342-222", "generic_name": "Memantine hydrochloride", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Memantine hydrochloride", "active_ingredients": [{"name": "MEMANTINE HYDROCHLORIDE", "strength": "28 mg/1"}], "application_number": "ANDA206310", "marketing_category": "ANDA", "marketing_start_date": "20250828", "listing_expiration_date": "20261231"}