Package 72162-1677-1

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1677-1
Digits Only 7216216771
Product NDC 72162-1677
Product ID 72162-1677_2530ad68-027f-4560-bb86-45c1452d9d30
Description

100 TABLET, FILM COATED in 1 BOTTLE (72162-1677-1)

Marketing

Marketing Status
Marketed Since 2019-11-22
Brand labetalol hydrochloride
Generic labetalol hydrochloride
Sample Package No

Linked Drug Pages (1)

Labetalol Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2530ad68-027f-4560-bb86-45c1452d9d30", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["R5H8897N95"], "rxcui": ["896766"], "spl_set_id": ["f7f7fade-98a6-4741-bfb9-f1eb54ad4565"], "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 (72162-1677-1)", "package_ndc": "72162-1677-1", "marketing_start_date": "20191122"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72162-1677-5)", "package_ndc": "72162-1677-5", "marketing_start_date": "20191122"}], "brand_name": "Labetalol Hydrochloride", "product_id": "72162-1677_2530ad68-027f-4560-bb86-45c1452d9d30", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72162-1677", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL", "strength": "300 mg/1"}], "application_number": "ANDA075215", "marketing_category": "ANDA", "marketing_start_date": "20191122", "listing_expiration_date": "20261231"}