Package 68788-8595-9

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68788-8595-9
Digits Only 6878885959
Product NDC 68788-8595
Description

90 TABLET in 1 BOTTLE (68788-8595-9)

Marketing

Marketing Status
Marketed Since 2024-03-01
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": "fc5cc977-a36b-4324-a4a6-7cfbd1fb0363", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856457"], "spl_set_id": ["1791ef4d-b609-41c8-b4ef-15bff752ddd7"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8595-3)", "package_ndc": "68788-8595-3", "marketing_start_date": "20240301"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8595-9)", "package_ndc": "68788-8595-9", "marketing_start_date": "20240301"}], "brand_name": "Propranolol Hydrochloride", "product_id": "68788-8595_fc5cc977-a36b-4324-a4a6-7cfbd1fb0363", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "68788-8595", "generic_name": "Propranolol Hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA071972", "marketing_category": "ANDA", "marketing_start_date": "20240301", "listing_expiration_date": "20261231"}