Package 60760-991-90

Brand: labetalol hydrochloride

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-991-90
Digits Only 6076099190
Product NDC 60760-991
Product ID 60760-991_302822c4-c396-167c-e063-6294a90a480b
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-991-90)

Marketing

Marketing Status
Marketed Since 2025-03-12
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": "302822c4-c396-167c-e063-6294a90a480b", "openfda": {"unii": ["1GEV3BAW9J"], "rxcui": ["896758"], "spl_set_id": ["30281c4d-2fd1-167a-e063-6294a90a77c4"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-991-90)", "package_ndc": "60760-991-90", "marketing_start_date": "20250312"}], "brand_name": "Labetalol Hydrochloride", "product_id": "60760-991_302822c4-c396-167c-e063-6294a90a480b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "60760-991", "generic_name": "Labetalol Hydrochloride", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA209603", "marketing_category": "ANDA", "marketing_start_date": "20210527", "listing_expiration_date": "20261231"}