Package 29300-254-05

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 29300-254-05
Digits Only 2930025405
Product NDC 29300-254
Product ID 29300-254_8325a41d-d05c-4c6b-b2fc-260c9380bfba
Description

500 TABLET, FILM COATED in 1 BOTTLE (29300-254-05)

Marketing

Marketing Status
Marketed Since 2022-10-01
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": "8325a41d-d05c-4c6b-b2fc-260c9380bfba", "openfda": {"upc": ["0329300254013"], "unii": ["1GEV3BAW9J"], "rxcui": ["896758", "896762", "896766"], "spl_set_id": ["ed0188ba-3fd3-4680-a829-ba242a115fab"], "manufacturer_name": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (29300-254-01)", "package_ndc": "29300-254-01", "marketing_start_date": "20221001"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (29300-254-05)", "package_ndc": "29300-254-05", "marketing_start_date": "20221001"}], "brand_name": "Labetalol Hydrochloride", "product_id": "29300-254_8325a41d-d05c-4c6b-b2fc-260c9380bfba", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "29300-254", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA212719", "marketing_category": "ANDA", "marketing_start_date": "20221001", "listing_expiration_date": "20271231"}