Package 51991-820-05

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51991-820-05
Digits Only 5199182005
Product NDC 51991-820
Product ID 51991-820_f7b4203a-c93c-47a2-9ad0-41df7d7a2c26
Description

500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51991-820-05)

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": "f7b4203a-c93c-47a2-9ad0-41df7d7a2c26", "openfda": {"upc": ["0351991819011", "0351991818014", "0351991820017"], "unii": ["F8A3652H1V"], "rxcui": ["856460", "856481", "856535", "856569"], "spl_set_id": ["179e31a7-9956-4fba-9e9a-2ca28d37d42b"], "manufacturer_name": ["Breckenridge Pharmaceutical, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51991-820-01)", "package_ndc": "51991-820-01", "marketing_start_date": "20130311"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (51991-820-05)", "package_ndc": "51991-820-05", "marketing_start_date": "20130311"}], "brand_name": "propranolol hydrochloride", "product_id": "51991-820_f7b4203a-c93c-47a2-9ad0-41df7d7a2c26", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "51991-820", "generic_name": "propranolol hydrochloride", "labeler_name": "Breckenridge Pharmaceutical, Inc.", "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"}