Package 51662-1338-1

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51662-1338-1
Digits Only 5166213381
Product NDC 51662-1338
Description

1 mL in 1 VIAL (51662-1338-1)

Marketing

Marketing Status
Marketed Since 2018-12-22
Brand propranolol hydrochloride
Generic propranolol hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "37b5006f-2441-f90b-e063-6294a90abb12", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856443"], "spl_set_id": ["7da73cee-4e98-462d-e053-2991aa0a8bf4"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL (51662-1338-1)", "package_ndc": "51662-1338-1", "marketing_start_date": "20181222"}, {"sample": false, "description": "10 POUCH in 1 CASE (51662-1338-3)  / 1 VIAL in 1 POUCH (51662-1338-2)  / 1 mL in 1 VIAL", "package_ndc": "51662-1338-3", "marketing_start_date": "20221001"}], "brand_name": "PROPRANOLOL HYDROCHLORIDE", "product_id": "51662-1338_37b5006f-2441-f90b-e063-6294a90abb12", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "51662-1338", "generic_name": "PROPRANOLOL HYDROCHLORIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROPRANOLOL HYDROCHLORIDE", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA077760", "marketing_category": "ANDA", "marketing_start_date": "20181222", "listing_expiration_date": "20261231"}