Package 23155-725-01

{"route": ["ORAL"], "spl_id": "c380ee30-4c39-4c05-a0e4-277b677902ae", "openfda": {"upc": ["0323155725018", "0323155724011", "0323155723014"], "unii": ["1GEV3BAW9J"], "spl_set_id": ["bf84ebae-3c91-4448-b1db-8e5ed3053866"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (23155-725-01)", "package_ndc": "23155-725-01", "marketing_start_date": "20200222"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (23155-725-05)", "package_ndc": "23155-725-05", "marketing_start_date": "20200222"}], "brand_name": "Labetalol Hydrochloride", "product_id": "23155-725_c380ee30-4c39-4c05-a0e4-277b677902ae", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "23155-725", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA074787", "marketing_category": "ANDA", "marketing_start_date": "20200222", "listing_expiration_date": "20271231"}