Package 68462-338-01

{"route": ["ORAL"], "spl_id": "b5186569-6be5-4ff2-a95e-f162f76254d9", "openfda": {"upc": ["0368462338018", "0368462337011", "0368462914014", "0368462336014"], "unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["4c3eea71-a7a1-4eda-9871-034ddeb83ed6"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68462-338-01)", "package_ndc": "68462-338-01", "marketing_start_date": "20231106"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68462-338-05)", "package_ndc": "68462-338-05", "marketing_start_date": "20231106"}, {"sample": false, "description": "100 BLISTER PACK in 1 CARTON (68462-338-14)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "68462-338-14", "marketing_start_date": "20231106"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "68462-338_b5186569-6be5-4ff2-a95e-f162f76254d9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "68462-338", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA216350", "marketing_category": "ANDA", "marketing_start_date": "20231106", "listing_expiration_date": "20271231"}