Package 50090-7743-1

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7743-1
Digits Only 5009077431
Product NDC 50090-7743
Product ID 50090-7743_a968cc6f-0e61-4264-86de-cf26477b03a0
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-7743-1)

Marketing

Marketing Status
Marketed Since 2025-10-30
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": "a968cc6f-0e61-4264-86de-cf26477b03a0", "openfda": {"unii": ["1GEV3BAW9J"], "rxcui": ["896766"], "spl_set_id": ["d4364caf-46c6-4144-9ba5-2c561e4f3a95"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7743-1)", "package_ndc": "50090-7743-1", "marketing_start_date": "20251030"}], "brand_name": "Labetalol Hydrochloride", "product_id": "50090-7743_a968cc6f-0e61-4264-86de-cf26477b03a0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-7743", "generic_name": "Labetalol Hydrochloride", "labeler_name": "A-S Medication Solutions", "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"}