Package 67046-1657-3

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67046-1657-3
Digits Only 6704616573
Product NDC 67046-1657
Product ID 67046-1657_4a007f46-7676-35da-e063-6294a90af585
Description

30 TABLET in 1 BLISTER PACK (67046-1657-3)

Marketing

Marketing Status
Marketed Since 2026-02-04
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": "4a007f46-7676-35da-e063-6294a90af585", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856457"], "spl_set_id": ["4a006e05-b8c3-236c-e063-6294a90abf26"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1657-3)", "package_ndc": "67046-1657-3", "marketing_start_date": "20260204"}], "brand_name": "Propranolol Hydrochloride", "product_id": "67046-1657_4a007f46-7676-35da-e063-6294a90af585", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "67046-1657", "generic_name": "Propranolol Hydrochloride", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA078955", "marketing_category": "ANDA", "marketing_start_date": "20260204", "listing_expiration_date": "20271231"}