Package 70518-4201-0

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4201-0
Digits Only 7051842010
Product NDC 70518-4201
Product ID 70518-4201_3ff4f9b1-7aa2-e196-e063-6294a90ae2e6
Description

180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4201-0)

Marketing

Marketing Status
Marketed Since 2024-10-02
Brand labetalol hydrochloride
Generic labetalol hydrochloride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3ff4f9b1-7aa2-e196-e063-6294a90ae2e6", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["R5H8897N95"], "rxcui": ["896758"], "spl_set_id": ["e2e50571-d8c1-43e7-b90f-877ba1c35c9b"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4201-0)", "package_ndc": "70518-4201-0", "marketing_start_date": "20241002"}], "brand_name": "Labetalol Hydrochloride", "product_id": "70518-4201_3ff4f9b1-7aa2-e196-e063-6294a90ae2e6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-4201", "generic_name": "Labetalol Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "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": "20241002", "listing_expiration_date": "20261231"}