Package 72162-1605-1

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1605-1
Digits Only 7216216051
Product NDC 72162-1605
Product ID 72162-1605_4265740f-b920-52c9-e063-6294a90a3ee4
Description

100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72162-1605-1)

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": "4265740f-b920-52c9-e063-6294a90a3ee4", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856481"], "spl_set_id": ["5cf8d0a4-4e02-48f0-8d1f-564357b250c5"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72162-1605-1)", "package_ndc": "72162-1605-1", "marketing_start_date": "20130311"}], "brand_name": "propranolol hydrochloride", "product_id": "72162-1605_4265740f-b920-52c9-e063-6294a90a3ee4", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72162-1605", "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": "160 mg/1"}], "application_number": "ANDA078703", "marketing_category": "ANDA", "marketing_start_date": "20130311", "listing_expiration_date": "20261231"}