Package 17856-3728-1

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 17856-3728-1
Digits Only 1785637281
Product NDC 17856-3728
Product ID 17856-3728_35d2e40e-8f0d-ef2d-e063-6294a90aadc0
Description

72 CUP in 1 CASE (17856-3728-1) / 5 mL in 1 CUP

Marketing

Marketing Status
Marketed Since 2024-05-10
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": "35d2e40e-8f0d-ef2d-e063-6294a90aadc0", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856724"], "spl_set_id": ["b609cc7c-1f6a-452b-8ada-c4d2989b83dc"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "72 CUP in 1 CASE (17856-3728-1)  / 5 mL in 1 CUP", "package_ndc": "17856-3728-1", "marketing_start_date": "20240510"}], "brand_name": "Propranolol Hydrochloride", "product_id": "17856-3728_35d2e40e-8f0d-ef2d-e063-6294a90aadc0", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "17856-3728", "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"}