Package 60760-545-60

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-545-60
Digits Only 6076054560
Product NDC 60760-545
Description

60 TABLET in 1 BOTTLE, PLASTIC (60760-545-60)

Marketing

Marketing Status
Marketed Since 2021-04-08
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": "c01fcaf6-a434-ec9a-e053-2995a90a0b65", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856457"], "spl_set_id": ["c01fc93e-cff2-50d5-e053-2a95a90a1897"], "manufacturer_name": ["St. Mary's Medical Park Pharmacy"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (60760-545-60)", "package_ndc": "60760-545-60", "marketing_start_date": "20210408"}], "brand_name": "Propranolol Hydrochloride", "product_id": "60760-545_c01fcaf6-a434-ec9a-e053-2995a90a0b65", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "60760-545", "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": "ANDA070322", "marketing_category": "ANDA", "marketing_start_date": "20210408", "listing_expiration_date": "20261231"}