Package 67296-2156-1

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67296-2156-1
Digits Only 6729621561
Product NDC 67296-2156
Product ID 67296-2156_45d26aad-d9c8-19f8-e063-6394a90a63c3
Description

15 TABLET, FILM COATED in 1 BOTTLE (67296-2156-1)

Marketing

Marketing Status
Marketed Since 2021-08-18
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": "45d26aad-d9c8-19f8-e063-6394a90a63c3", "openfda": {"upc": ["0372888120010", "0372888120058", "0372888121055", "0372888122014", "0372888122052", "0372888121017"], "unii": ["1GEV3BAW9J"], "rxcui": ["896758"], "spl_set_id": ["32525ed4-3cca-2b99-e063-6294a90a6c66"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (67296-2156-1)", "package_ndc": "67296-2156-1", "marketing_start_date": "20210818"}], "brand_name": "LABETALOL HYDROCHLORIDE", "product_id": "67296-2156_45d26aad-d9c8-19f8-e063-6394a90a63c3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "67296-2156", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Redpharm Drug", "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": "20210818", "listing_expiration_date": "20261231"}