Package 63629-1166-1

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-1166-1
Digits Only 6362911661
Product NDC 63629-1166
Product ID 63629-1166_bd6d03a3-c34b-4817-a263-0bc27dd645fa
Description

500 TABLET, FILM COATED in 1 BOTTLE (63629-1166-1)

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": "bd6d03a3-c34b-4817-a263-0bc27dd645fa", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["R5H8897N95"], "rxcui": ["896766"], "spl_set_id": ["5a39bb96-4a60-49e8-859c-16bda0fe18e4"], "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": "500 TABLET, FILM COATED in 1 BOTTLE (63629-1166-1)", "package_ndc": "63629-1166-1", "marketing_start_date": "20191122"}], "brand_name": "Labetalol Hydrochloride", "product_id": "63629-1166_bd6d03a3-c34b-4817-a263-0bc27dd645fa", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "63629-1166", "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"}