Package 43353-961-60

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43353-961-60
Digits Only 4335396160
Product NDC 43353-961
Description

90 TABLET in 1 BOTTLE, PLASTIC (43353-961-60)

Marketing

Marketing Status
Marketed Since 2014-09-11
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": "49006163-8921-6eaf-e063-6394a90a39c2", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856457", "856519"], "spl_set_id": ["7da9bb37-cc22-4eff-8de0-429f64cb599e"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (43353-961-60)", "package_ndc": "43353-961-60", "marketing_start_date": "20140911"}], "brand_name": "Propranolol Hydrochloride", "product_id": "43353-961_49006163-8921-6eaf-e063-6394a90a39c2", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "43353-961", "generic_name": "propranolol hydrochloride", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA070213", "marketing_category": "ANDA", "marketing_start_date": "19851119", "listing_expiration_date": "20271231"}