Package 51662-1602-1
Brand: labetalol hcl
Generic: labetalol hclPackage Facts
Identity
Package NDC
51662-1602-1
Digits Only
5166216021
Product NDC
51662-1602
Description
1 VIAL in 1 BOX, UNIT-DOSE (51662-1602-1) / 20 mL in 1 VIAL
Marketing
Marketing Status
Brand
labetalol hcl
Generic
labetalol hcl
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "ea035948-1a97-5d6e-e053-2995a90a3e7b", "openfda": {"unii": ["1GEV3BAW9J"], "rxcui": ["896771"], "spl_set_id": ["e76c4b37-4a34-249d-e053-2995a90aa9be"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX, UNIT-DOSE (51662-1602-1) / 20 mL in 1 VIAL", "package_ndc": "51662-1602-1", "marketing_start_date": "20220829"}, {"sample": false, "description": "20 mL in 1 VIAL (51662-1602-9)", "package_ndc": "51662-1602-9", "marketing_start_date": "20221001"}], "brand_name": "LABETALOL HCl", "product_id": "51662-1602_ea035948-1a97-5d6e-e053-2995a90a3e7b", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "51662-1602", "generic_name": "LABETALOL HCl", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LABETALOL HCl", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "5 mg/mL"}], "application_number": "ANDA075303", "marketing_category": "ANDA", "marketing_start_date": "20220829", "listing_expiration_date": "20261231"}