Package 71335-2876-1

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2876-1
Digits Only 7133528761
Product NDC 71335-2876
Product ID 71335-2876_4253c88e-7b74-695b-e063-6394a90a6b6b
Description

100 TABLET, FILM COATED in 1 BOTTLE (71335-2876-1)

Marketing

Marketing Status
Marketed Since 2025-10-29
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": "4253c88e-7b74-695b-e063-6394a90a6b6b", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["R5H8897N95"], "rxcui": ["896762"], "spl_set_id": ["0dcd514d-bda8-484b-8cf1-f5656aaab9ce"], "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 (71335-2876-1)", "package_ndc": "71335-2876-1", "marketing_start_date": "20251029"}], "brand_name": "Labetalol Hydrochloride", "product_id": "71335-2876_4253c88e-7b74-695b-e063-6394a90a6b6b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71335-2876", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL", "strength": "200 mg/1"}], "application_number": "ANDA075215", "marketing_category": "ANDA", "marketing_start_date": "20191122", "listing_expiration_date": "20261231"}