Package 17856-8728-1

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 17856-8728-1
Digits Only 1785687281
Product NDC 17856-8728
Product ID 17856-8728_40333fbc-1ccd-7a2c-e063-6294a90a8bc9
Description

50 CUP in 1 CASE (17856-8728-1) / 5 mL in 1 CUP

Marketing

Marketing Status
Marketed Since 2025-10-01
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": "40333fbc-1ccd-7a2c-e063-6294a90a8bc9", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856724"], "spl_set_id": ["40333bee-749f-0b43-e063-6394a90a149c"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "50 CUP in 1 CASE (17856-8728-1)  / 5 mL in 1 CUP", "package_ndc": "17856-8728-1", "marketing_start_date": "20251001"}], "brand_name": "Propranolol Hydrochloride", "product_id": "17856-8728_40333fbc-1ccd-7a2c-e063-6294a90a8bc9", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "17856-8728", "generic_name": "Propranolol Hydrochloride", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "20 mg/5mL"}], "application_number": "ANDA070979", "marketing_category": "ANDA", "marketing_start_date": "19870515", "listing_expiration_date": "20261231"}