Package 0054-3730-63

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0054-3730-63
Digits Only 0054373063
Product NDC 0054-3730
Description

500 mL in 1 BOTTLE, PLASTIC (0054-3730-63)

Marketing

Marketing Status
Marketed Since 1987-05-15
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": "245a43cc-cbf8-486d-ad3c-724aca63fd72", "openfda": {"upc": ["0300543730632", "0300543727632"], "unii": ["F8A3652H1V"], "rxcui": ["856724", "856733"], "spl_set_id": ["8fe0a04c-bf5b-4ba0-9df6-58c27f24b52e"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 mL in 1 BOTTLE, PLASTIC (0054-3730-63)", "package_ndc": "0054-3730-63", "marketing_start_date": "19870515"}], "brand_name": "Propranolol Hydrochloride", "product_id": "0054-3730_245a43cc-cbf8-486d-ad3c-724aca63fd72", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0054-3730", "generic_name": "Propranolol Hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "40 mg/5mL"}], "application_number": "ANDA070690", "marketing_category": "ANDA", "marketing_start_date": "19870515", "listing_expiration_date": "20261231"}