Package 50090-7101-1

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7101-1
Digits Only 5009071011
Product NDC 50090-7101
Description

100 TABLET in 1 BOTTLE (50090-7101-1)

Marketing

Marketing Status
Marketed Since 2024-02-29
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": "e066fdd7-a8bc-4cc5-88e6-1c6556bac6dd", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856457"], "spl_set_id": ["325dda2c-ecd9-4368-8779-7ff505b2b138"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-7101-1)", "package_ndc": "50090-7101-1", "marketing_start_date": "20240229"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7101-6)", "package_ndc": "50090-7101-6", "marketing_start_date": "20240229"}], "brand_name": "Propranolol Hydrochloride", "product_id": "50090-7101_e066fdd7-a8bc-4cc5-88e6-1c6556bac6dd", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-7101", "generic_name": "Propranolol Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA071972", "marketing_category": "ANDA", "marketing_start_date": "20210603", "listing_expiration_date": "20261231"}