Package 72162-1604-1

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1604-1
Digits Only 7216216041
Product NDC 72162-1604
Product ID 72162-1604_426569c9-2a1b-67ec-e063-6294a90a6941
Description

100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72162-1604-1)

Marketing

Marketing Status
Marketed Since 2013-03-11
Brand propranolol hydrochloride
Generic propranolol hydrochloride
Sample Package No

Linked Drug Pages (1)

propranolol hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "426569c9-2a1b-67ec-e063-6294a90a6941", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856460"], "spl_set_id": ["96fa108c-b31c-445c-b978-c848cac59419"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72162-1604-1)", "package_ndc": "72162-1604-1", "marketing_start_date": "20130311"}], "brand_name": "propranolol hydrochloride", "product_id": "72162-1604_426569c9-2a1b-67ec-e063-6294a90a6941", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72162-1604", "generic_name": "propranolol hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "propranolol hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA078703", "marketing_category": "ANDA", "marketing_start_date": "20130311", "listing_expiration_date": "20261231"}