Package 0228-2779-11

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0228-2779-11
Digits Only 0228277911
Product NDC 0228-2779
Description

100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0228-2779-11)

Marketing

Marketing Status
Marketed Since 2007-08-10
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": "1f70f68b-1314-4c20-872e-993e0f33fb43", "openfda": {"upc": ["0302282780114"], "unii": ["F8A3652H1V"], "rxcui": ["856460", "856481", "856535", "856569"], "spl_set_id": ["a4edba76-29b8-41fb-bf0b-d4633abba003"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0228-2779-11)", "package_ndc": "0228-2779-11", "marketing_start_date": "20070810"}], "brand_name": "Propranolol Hydrochloride", "product_id": "0228-2779_1f70f68b-1314-4c20-872e-993e0f33fb43", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0228-2779", "generic_name": "Propranolol Hydrochloride", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA078494", "marketing_category": "ANDA", "marketing_start_date": "20070810", "listing_expiration_date": "20261231"}