Package 72189-074-30

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72189-074-30
Digits Only 7218907430
Product NDC 72189-074
Product ID 72189-074_2be818df-f32a-45a2-e063-6294a90a334a
Description

30 TABLET in 1 BOTTLE (72189-074-30)

Marketing

Marketing Status
Marketed Since 2020-06-16
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": "2be818df-f32a-45a2-e063-6294a90a334a", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856448"], "spl_set_id": ["a834d1cf-72fc-93bf-e053-2995a90a6191"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-074-30)", "package_ndc": "72189-074-30", "marketing_start_date": "20200616"}], "brand_name": "PROPRANOLOL HYDROCHLORIDE", "product_id": "72189-074_2be818df-f32a-45a2-e063-6294a90a334a", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72189-074", "generic_name": "PROPRANOLOL HYDROCHLORIDE", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROPRANOLOL HYDROCHLORIDE", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA070217", "marketing_category": "ANDA", "marketing_start_date": "20200616", "listing_expiration_date": "20261231"}