Package 71335-1242-1

{"route": ["ORAL"], "spl_id": "f2ab8c44-59a2-4c4b-abc1-2e6a4e8b2b5c", "openfda": {"unii": ["1GEV3BAW9J"], "rxcui": ["896762"], "spl_set_id": ["9c3bb751-c425-43ff-b530-2460b568b689"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-1242-1)", "package_ndc": "71335-1242-1", "marketing_start_date": "20191127"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-1242-2)", "package_ndc": "71335-1242-2", "marketing_start_date": "20210723"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-1242-3)", "package_ndc": "71335-1242-3", "marketing_start_date": "20190606"}], "brand_name": "Labetalol Hydrochloride", "product_id": "71335-1242_f2ab8c44-59a2-4c4b-abc1-2e6a4e8b2b5c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71335-1242", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA207743", "marketing_category": "ANDA", "marketing_start_date": "20171205", "listing_expiration_date": "20261231"}