Package 72162-1602-1
Brand: propranolol hydrochloride
Generic: propranolol hydrochloridePackage Facts
Identity
Package NDC
72162-1602-1
Digits Only
7216216021
Product NDC
72162-1602
Description
100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72162-1602-1)
Marketing
Marketing Status
Brand
propranolol hydrochloride
Generic
propranolol hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "42654a6a-dc45-f46d-e063-6394a90a93e2", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856535"], "spl_set_id": ["1aedd4d5-fe70-4cb0-9d6d-d2bd241ebaa6"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72162-1602-1)", "package_ndc": "72162-1602-1", "marketing_start_date": "20130311"}], "brand_name": "propranolol hydrochloride", "product_id": "72162-1602_42654a6a-dc45-f46d-e063-6394a90a93e2", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72162-1602", "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": "60 mg/1"}], "application_number": "ANDA078703", "marketing_category": "ANDA", "marketing_start_date": "20130311", "listing_expiration_date": "20261231"}