Package 71872-7096-1

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71872-7096-1
Digits Only 7187270961
Product NDC 71872-7096
Description

1 VIAL in 1 BAG (71872-7096-1) / 1 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2018-03-30
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": "fc5e5df1-f935-b388-e053-6394a90a37ab", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856443"], "spl_set_id": ["693569bd-6053-5b3e-e053-2a91aa0a6e9c"], "manufacturer_name": ["Medical Purchasing Solutions, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BAG (71872-7096-1)  / 1 mL in 1 VIAL", "package_ndc": "71872-7096-1", "marketing_start_date": "20180330"}], "brand_name": "Propranolol Hydrochloride", "product_id": "71872-7096_fc5e5df1-f935-b388-e053-6394a90a37ab", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71872-7096", "generic_name": "Propranolol Hydrochloride", "labeler_name": "Medical Purchasing Solutions, LLC", "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": "20080131", "listing_expiration_date": "20261231"}