Package 33342-515-11

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 33342-515-11
Digits Only 3334251511
Product NDC 33342-515
Product ID 33342-515_366134cd-6244-45fc-99f1-0193a0221b3a
Description

100 TABLET, FILM COATED in 1 BOTTLE (33342-515-11)

Marketing

Marketing Status
Marketed Since 2025-09-23
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": "366134cd-6244-45fc-99f1-0193a0221b3a", "openfda": {"upc": ["0333342516114", "0333342515155", "0333342517111"], "unii": ["1GEV3BAW9J"], "rxcui": ["896758", "896762", "896766"], "spl_set_id": ["366134cd-6244-45fc-99f1-0193a0221b3a"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (33342-515-11)", "package_ndc": "33342-515-11", "marketing_start_date": "20250923"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (33342-515-15)", "package_ndc": "33342-515-15", "marketing_start_date": "20250923"}], "brand_name": "Labetalol Hydrochloride", "product_id": "33342-515_366134cd-6244-45fc-99f1-0193a0221b3a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "33342-515", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA217949", "marketing_category": "ANDA", "marketing_start_date": "20250923", "listing_expiration_date": "20261231"}