Package 50090-7618-6

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 50090-7618-6
Digits Only 5009076186
Product NDC 50090-7618
Description

90 TABLET in 1 BOTTLE (50090-7618-6)

Marketing

Marketing Status
Marketed Since 2025-08-01
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": "cc40a50e-44b2-4146-9796-b390066072fb", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856519"], "spl_set_id": ["be55cf2d-c2f8-4781-b2ef-fd607324265c"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-7618-1)", "package_ndc": "50090-7618-1", "marketing_start_date": "20250801"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7618-6)", "package_ndc": "50090-7618-6", "marketing_start_date": "20250801"}], "brand_name": "Propranolol Hydrochloride", "product_id": "50090-7618_cc40a50e-44b2-4146-9796-b390066072fb", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-7618", "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": "40 mg/1"}], "application_number": "ANDA078955", "marketing_category": "ANDA", "marketing_start_date": "20240919", "listing_expiration_date": "20261231"}