Package 67296-2114-6

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67296-2114-6
Digits Only 6729621146
Product NDC 67296-2114
Product ID 67296-2114_3b0aa187-8058-8e3b-e063-6294a90a373e
Description

60 TABLET, FILM COATED in 1 BOTTLE (67296-2114-6)

Marketing

Marketing Status
Marketed Since 2021-05-27
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": "3b0aa187-8058-8e3b-e063-6294a90a373e", "openfda": {"upc": ["0370377061134", "0370377060120"], "unii": ["1GEV3BAW9J"], "rxcui": ["896766"], "spl_set_id": ["1e1b7355-4802-d277-e063-6394a90aef44"], "manufacturer_name": ["RedPharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET, FILM COATED in 1 BOTTLE (67296-2114-2)", "package_ndc": "67296-2114-2", "marketing_start_date": "20210527"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (67296-2114-6)", "package_ndc": "67296-2114-6", "marketing_start_date": "20210527"}], "brand_name": "Labetalol Hydrochloride", "product_id": "67296-2114_3b0aa187-8058-8e3b-e063-6294a90a373e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "67296-2114", "generic_name": "Labetalol Hydrochloride", "labeler_name": "RedPharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA209603", "marketing_category": "ANDA", "marketing_start_date": "20210527", "listing_expiration_date": "20261231"}