Package 60760-628-90

Brand: labetalol hcl

Generic: labetalol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-628-90
Digits Only 6076062890
Product NDC 60760-628
Product ID 60760-628_c8ad3090-0526-6aa5-e053-2a95a90a65cc
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-628-90)

Marketing

Marketing Status
Marketed Since 2021-07-27
Brand labetalol hcl
Generic labetalol hydrochloride
Sample Package No

Linked Drug Pages (1)

Labetalol HCL ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c8ad3090-0526-6aa5-e053-2a95a90a65cc", "openfda": {"unii": ["1GEV3BAW9J"], "rxcui": ["896758"], "spl_set_id": ["c8ad238a-0c94-28ea-e053-2995a90a778d"], "manufacturer_name": ["St. Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-628-90)", "package_ndc": "60760-628-90", "marketing_start_date": "20210727"}], "brand_name": "Labetalol HCL", "product_id": "60760-628_c8ad3090-0526-6aa5-e053-2a95a90a65cc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "60760-628", "generic_name": "Labetalol Hydrochloride", "labeler_name": "St. Mary's Medical Park Pharmacy", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol HCL", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA200908", "marketing_category": "ANDA", "marketing_start_date": "20210727", "listing_expiration_date": "20261231"}