Package 70518-3499-1

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3499-1
Digits Only 7051834991
Product NDC 70518-3499
Product ID 70518-3499_3aada26e-6a8c-f545-e063-6394a90a9f80
Description

180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3499-1)

Marketing

Marketing Status
Marketed Since 2022-09-20
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": "3aada26e-6a8c-f545-e063-6394a90a9f80", "openfda": {"unii": ["1GEV3BAW9J"], "rxcui": ["896758"], "spl_set_id": ["ae5d7b3b-e444-48d3-9d85-9b07319f9374"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3499-0)", "package_ndc": "70518-3499-0", "marketing_start_date": "20220825"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3499-1)", "package_ndc": "70518-3499-1", "marketing_start_date": "20220920"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3499-2)", "package_ndc": "70518-3499-2", "marketing_start_date": "20220920"}], "brand_name": "LABETALOL HYDROCHLORIDE", "product_id": "70518-3499_3aada26e-6a8c-f545-e063-6394a90a9f80", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-3499", "generic_name": "Labetalol Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LABETALOL HYDROCHLORIDE", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA211953", "marketing_category": "ANDA", "marketing_start_date": "20220825", "listing_expiration_date": "20261231"}