Package 71205-095-60

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71205-095-60
Digits Only 7120509560
Product NDC 71205-095
Description

60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-095-60)

Marketing

Marketing Status
Marketed Since 2018-08-01
Brand labetalol hydrochloride
Generic labetalol hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5179866d-f336-4e03-85b0-972fbedb6b9e", "openfda": {"upc": ["0371205095901"], "unii": ["1GEV3BAW9J"], "rxcui": ["896758"], "spl_set_id": ["c0301841-e209-4242-bace-58a20e6dd01b"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-095-30)", "package_ndc": "71205-095-30", "marketing_start_date": "20180801"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-095-60)", "package_ndc": "71205-095-60", "marketing_start_date": "20180801"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-095-90)", "package_ndc": "71205-095-90", "marketing_start_date": "20180801"}], "brand_name": "Labetalol hydrochloride", "product_id": "71205-095_5179866d-f336-4e03-85b0-972fbedb6b9e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71205-095", "generic_name": "Labetalol hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol hydrochloride", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA075133", "marketing_category": "ANDA", "marketing_start_date": "19980803", "listing_expiration_date": "20261231"}