Package 60760-589-30

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-589-30
Digits Only 6076058930
Product NDC 60760-589
Product ID 60760-589_48ec8807-74d2-1248-e063-6394a90a4418
Description

30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-589-30)

Marketing

Marketing Status
Marketed Since 2024-03-15
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": "48ec8807-74d2-1248-e063-6394a90a4418", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856569"], "spl_set_id": ["14957737-4e53-cc6d-e063-6294a90a181e"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-589-30)", "package_ndc": "60760-589-30", "marketing_start_date": "20240315"}], "brand_name": "propranolol hydrochloride", "product_id": "60760-589_48ec8807-74d2-1248-e063-6394a90a4418", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "60760-589", "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": "80 mg/1"}], "application_number": "ANDA078703", "marketing_category": "ANDA", "marketing_start_date": "20130311", "listing_expiration_date": "20271231"}