Package 55154-8192-0

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55154-8192-0
Digits Only 5515481920
Product NDC 55154-8192
Product ID 55154-8192_9be82c15-a0ba-4f52-8e76-6700731db35e
Description

10 BLISTER PACK in 1 BAG (55154-8192-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2019-07-16
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": "9be82c15-a0ba-4f52-8e76-6700731db35e", "openfda": {"upc": ["0055154214308", "0055154819206"], "unii": ["1GEV3BAW9J"], "rxcui": ["896758", "896762"], "spl_set_id": ["63db5b00-e864-4b2d-84f2-00bf35211b9b"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-8192-0)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "55154-8192-0", "marketing_start_date": "20190716"}], "brand_name": "Labetalol Hydrochloride", "product_id": "55154-8192_9be82c15-a0ba-4f52-8e76-6700731db35e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "55154-8192", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA207743", "marketing_category": "ANDA", "marketing_start_date": "20190716", "listing_expiration_date": "20261231"}