Package 0603-5483-32

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0603-5483-32
Digits Only 0603548332
Product NDC 0603-5483
Product ID 0603-5483_2d7e19e5-6f01-4657-a201-829ea5a74f84
Description

1000 TABLET in 1 BOTTLE (0603-5483-32)

Marketing

Marketing Status
Marketed Since 2010-06-21
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": "2d7e19e5-6f01-4657-a201-829ea5a74f84", "openfda": {"upc": ["0306035482218", "0306035485219", "0306035483215", "0306035486216", "0306035484212"], "unii": ["F8A3652H1V"], "rxcui": ["856448", "856457", "856519", "856556", "856578"], "spl_set_id": ["0d74bb04-8227-4afa-b523-ce1556150e07"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0603-5483-21)", "package_ndc": "0603-5483-21", "marketing_start_date": "20100621"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (0603-5483-32)", "package_ndc": "0603-5483-32", "marketing_start_date": "20100621"}], "brand_name": "Propranolol Hydrochloride", "product_id": "0603-5483_2d7e19e5-6f01-4657-a201-829ea5a74f84", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0603-5483", "generic_name": "propranolol hydrochloride", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA070221", "marketing_category": "ANDA", "marketing_start_date": "20100621", "listing_expiration_date": "20261231"}