Package 71335-0554-6

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-0554-6
Digits Only 7133505546
Product NDC 71335-0554
Product ID 71335-0554_5b7d1148-a500-43c2-aefd-b8ac3aa2e6bc
Description

10 TABLET in 1 BOTTLE (71335-0554-6)

Marketing

Marketing Status
Marketed Since 2016-10-10
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": "5b7d1148-a500-43c2-aefd-b8ac3aa2e6bc", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856448", "856457", "856519", "856578"], "spl_set_id": ["360de855-b8be-409f-9ca6-d0a0368af174"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0554-1)", "package_ndc": "71335-0554-1", "marketing_start_date": "20161010"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0554-2)", "package_ndc": "71335-0554-2", "marketing_start_date": "20161010"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-0554-3)", "package_ndc": "71335-0554-3", "marketing_start_date": "20161010"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0554-4)", "package_ndc": "71335-0554-4", "marketing_start_date": "20161010"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-0554-5)", "package_ndc": "71335-0554-5", "marketing_start_date": "20161010"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-0554-6)", "package_ndc": "71335-0554-6", "marketing_start_date": "20161010"}], "brand_name": "Propranolol Hydrochloride", "product_id": "71335-0554_5b7d1148-a500-43c2-aefd-b8ac3aa2e6bc", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71335-0554", "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": "10 mg/1"}], "application_number": "ANDA070221", "marketing_category": "ANDA", "marketing_start_date": "20100621", "listing_expiration_date": "20261231"}