Package 82868-003-30

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82868-003-30
Digits Only 8286800330
Product NDC 82868-003
Description

30 TABLET in 1 BOTTLE, PLASTIC (82868-003-30)

Marketing

Marketing Status
Marketed Since 2023-08-15
Brand propranolol hydrochloride
Generic propranolol hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "46dc87c7-cc52-3e0c-e063-6294a90aff3e", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856457"], "spl_set_id": ["03afbc5a-a9dc-e823-e063-6394a90a0cb2"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (82868-003-30)", "package_ndc": "82868-003-30", "marketing_start_date": "20230815"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (82868-003-90)", "package_ndc": "82868-003-90", "marketing_start_date": "20240429"}], "brand_name": "Propranolol Hydrochloride", "product_id": "82868-003_46dc87c7-cc52-3e0c-e063-6294a90aff3e", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "82868-003", "generic_name": "Propranolol Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA071972", "marketing_category": "ANDA", "marketing_start_date": "20230815", "listing_expiration_date": "20261231"}