Package 67046-1582-3

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67046-1582-3
Digits Only 6704615823
Product NDC 67046-1582
Product ID 67046-1582_3e5003d5-cec7-4696-e063-6294a90abe36
Description

30 TABLET in 1 BLISTER PACK (67046-1582-3)

Marketing

Marketing Status
Marketed Since 2025-09-08
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": "3e5003d5-cec7-4696-e063-6294a90abe36", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856556"], "spl_set_id": ["3e50045f-abdf-3b78-e063-6394a90a4ba0"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1582-3)", "package_ndc": "67046-1582-3", "marketing_start_date": "20250908"}], "brand_name": "Propranolol Hydrochloride", "product_id": "67046-1582_3e5003d5-cec7-4696-e063-6294a90abe36", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "67046-1582", "generic_name": "Propranolol Hydrochloride", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA071976", "marketing_category": "ANDA", "marketing_start_date": "20250908", "listing_expiration_date": "20261231"}