Package 72162-1675-1
Brand: labetalol hydrochloride
Generic: labetalol hydrochloridePackage Facts
Identity
Package NDC
72162-1675-1
Digits Only
7216216751
Product NDC
72162-1675
Description
100 TABLET, FILM COATED in 1 BOTTLE (72162-1675-1)
Marketing
Marketing Status
Brand
labetalol hydrochloride
Generic
labetalol hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "80aece15-94da-4ce7-bf9d-7f423be5c591", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["R5H8897N95"], "rxcui": ["896758"], "spl_set_id": ["35e7bce0-d9ff-4f8b-95c5-218da2a2d929"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72162-1675-1)", "package_ndc": "72162-1675-1", "marketing_start_date": "20191122"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72162-1675-5)", "package_ndc": "72162-1675-5", "marketing_start_date": "20191122"}], "brand_name": "Labetalol Hydrochloride", "product_id": "72162-1675_80aece15-94da-4ce7-bf9d-7f423be5c591", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72162-1675", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL", "strength": "100 mg/1"}], "application_number": "ANDA075215", "marketing_category": "ANDA", "marketing_start_date": "20191122", "listing_expiration_date": "20261231"}