Package 71247-130-01

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71247-130-01
Digits Only 7124713001
Product NDC 71247-130
Product ID 71247-130_09304c97-8d53-4561-b157-765544fd362c
Description

100 TABLET, FILM COATED in 1 BOTTLE (71247-130-01)

Marketing

Marketing Status
Marketed Since 2021-02-08
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": "09304c97-8d53-4561-b157-765544fd362c", "openfda": {"upc": ["0371247126014", "0371247127011", "0371247130011"], "unii": ["1GEV3BAW9J"], "rxcui": ["896758", "896762", "896766"], "spl_set_id": ["82fc2d64-0572-4a9b-94fc-f6eb8d930c54"], "manufacturer_name": ["Innogenix, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71247-130-01)", "package_ndc": "71247-130-01", "marketing_start_date": "20210208"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (71247-130-05)", "package_ndc": "71247-130-05", "marketing_start_date": "20210208"}], "brand_name": "Labetalol Hydrochloride", "product_id": "71247-130_09304c97-8d53-4561-b157-765544fd362c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71247-130", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Innogenix, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA075215", "marketing_category": "ANDA", "marketing_start_date": "20210208", "listing_expiration_date": "20261231"}