Package 0121-0646-10

{"route": ["ORAL"], "spl_id": "0d5911e6-e5b6-4013-98ec-773d9ec62dec", "openfda": {"unii": ["M6Q1EO9TD0"], "rxcui": ["849385"], "spl_set_id": ["be411327-5ac7-46df-b5e4-32a11b419b15"], "manufacturer_name": ["PAI Holdings, LLC dba PAI Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TRAY in 1 CASE (0121-0646-10)  / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE", "package_ndc": "0121-0646-10", "marketing_start_date": "19950717"}, {"sample": false, "description": "473 mL in 1 BOTTLE (0121-0646-16)", "package_ndc": "0121-0646-16", "marketing_start_date": "19950717"}], "brand_name": "AMANTADINE HYDROCHLORIDE", "product_id": "0121-0646_0d5911e6-e5b6-4013-98ec-773d9ec62dec", "dosage_form": "SOLUTION", "pharm_class": ["Influenza A M2 Protein Inhibitor [EPC]", "M2 Protein Inhibitors [MoA]"], "product_ndc": "0121-0646", "generic_name": "AMANTADINE HYDROCHLORIDE", "labeler_name": "PAI Holdings, LLC dba PAI Pharma", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMANTADINE HYDROCHLORIDE", "active_ingredients": [{"name": "AMANTADINE HYDROCHLORIDE", "strength": "50 mg/5mL"}], "application_number": "ANDA074509", "marketing_category": "ANDA", "marketing_start_date": "19950717", "listing_expiration_date": "20261231"}