Package 43063-647-30

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43063-647-30
Digits Only 4306364730
Product NDC 43063-647
Description

30 TABLET in 1 BOTTLE, PLASTIC (43063-647-30)

Marketing

Marketing Status
Marketed Since 2016-03-09
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": "2f3b1710-4cbb-8df1-e063-6294a90a7539", "openfda": {"upc": ["0343063647905"], "unii": ["F8A3652H1V"], "rxcui": ["856519"], "spl_set_id": ["29a3a271-dabc-437f-e054-00144ff8d46c"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-647-30)", "package_ndc": "43063-647-30", "marketing_start_date": "20160309"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (43063-647-90)", "package_ndc": "43063-647-90", "marketing_start_date": "20160309"}], "brand_name": "Propranolol Hydrochloride", "product_id": "43063-647_2f3b1710-4cbb-8df1-e063-6294a90a7539", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "43063-647", "generic_name": "propranolol hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA070221", "marketing_category": "ANDA", "marketing_start_date": "20100621", "listing_expiration_date": "20261231"}