Package 60760-731-60

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-731-60
Digits Only 6076073160
Product NDC 60760-731
Product ID 60760-731_42def69e-9eb7-af05-e063-6394a90a421c
Description

60 TABLET in 1 BOTTLE, PLASTIC (60760-731-60)

Marketing

Marketing Status
Marketed Since 2025-11-05
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": "42def69e-9eb7-af05-e063-6394a90a421c", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856457"], "spl_set_id": ["42def694-9484-a2ca-e063-6394a90a87d8"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (60760-731-60)", "package_ndc": "60760-731-60", "marketing_start_date": "20251105"}], "brand_name": "Propranolol Hydrochloride", "product_id": "60760-731_42def69e-9eb7-af05-e063-6394a90a421c", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "60760-731", "generic_name": "Propranolol Hydrochloride", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "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"}