Package 84549-604-01

Brand: propranolol

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 84549-604-01
Digits Only 8454960401
Product NDC 84549-604
Description

1 mL in 1 VIAL, SINGLE-DOSE (84549-604-01)

Marketing

Marketing Status
Marketed Since 2025-12-11
Brand propranolol
Generic propranolol hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "45b0aaf0-df6d-7db0-e063-6294a90a9135", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856443"], "spl_set_id": ["45b0aaf0-df6c-7db0-e063-6294a90a9135"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL, SINGLE-DOSE (84549-604-01)", "package_ndc": "84549-604-01", "marketing_start_date": "20251211"}], "brand_name": "Propranolol", "product_id": "84549-604_45b0aaf0-df6d-7db0-e063-6294a90a9135", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "84549-604", "generic_name": "PROPRANOLOL HYDROCHLORIDE", "labeler_name": "ProPharma Distribution", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA075826", "marketing_category": "ANDA", "marketing_start_date": "20010907", "listing_expiration_date": "20261231"}