Package 50090-7104-1
Brand: propranolol hydrochloride
Generic: propranolol hydrochloridePackage Facts
Identity
Package NDC
50090-7104-1
Digits Only
5009071041
Product NDC
50090-7104
Description
60 TABLET in 1 BOTTLE (50090-7104-1)
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": "1d38c2d9-7c4a-4449-b0d5-55131d43f3cb", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856519"], "spl_set_id": ["7b751df5-0751-435b-8755-3d50476cabd2"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-7104-1)", "package_ndc": "50090-7104-1", "marketing_start_date": "20240229"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-7104-6)", "package_ndc": "50090-7104-6", "marketing_start_date": "20240229"}], "brand_name": "Propranolol Hydrochloride", "product_id": "50090-7104_1d38c2d9-7c4a-4449-b0d5-55131d43f3cb", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "50090-7104", "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": "ANDA071972", "marketing_category": "ANDA", "marketing_start_date": "20210603", "listing_expiration_date": "20261231"}