Package 60760-867-30

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60760-867-30
Digits Only 6076086730
Product NDC 60760-867
Product ID 60760-867_36230ab7-356c-a3e6-e063-6294a90aaf6e
Description

30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-867-30)

Marketing

Marketing Status
Marketed Since 2025-05-19
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": "36230ab7-356c-a3e6-e063-6294a90aaf6e", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856535"], "spl_set_id": ["36230aaa-b6e5-4ebb-e063-6294a90ac3b9"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-867-30)", "package_ndc": "60760-867-30", "marketing_start_date": "20250519"}], "brand_name": "propranolol hydrochloride", "product_id": "60760-867_36230ab7-356c-a3e6-e063-6294a90aaf6e", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "60760-867", "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": "60 mg/1"}], "application_number": "ANDA078703", "marketing_category": "ANDA", "marketing_start_date": "20130311", "listing_expiration_date": "20261231"}