Package 71335-2299-1

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2299-1
Digits Only 7133522991
Product NDC 71335-2299
Product ID 71335-2299_0973b288-7f06-4c22-ae38-9fc16865d18f
Description

1000 TABLET in 1 BOTTLE (71335-2299-1)

Marketing

Marketing Status
Marketed Since 2024-10-04
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": "0973b288-7f06-4c22-ae38-9fc16865d18f", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856457"], "spl_set_id": ["89331052-2648-46c6-8d4c-7934ab1ee683"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (71335-2299-1)", "package_ndc": "71335-2299-1", "marketing_start_date": "20241004"}], "brand_name": "Propranolol Hydrochloride", "product_id": "71335-2299_0973b288-7f06-4c22-ae38-9fc16865d18f", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71335-2299", "generic_name": "propranolol hydrochloride", "labeler_name": "Bryant Ranch Prepack", "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"}