Package 70756-297-51

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70756-297-51
Digits Only 7075629751
Product NDC 70756-297
Description

500 TABLET in 1 BOTTLE (70756-297-51)

Marketing

Marketing Status
Marketed Since 2026-01-27
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": "f1ed91cc-9651-41e9-bc21-855bdf78e5fc", "openfda": {"upc": ["0370756296119", "0370756296126", "0370756095118"], "unii": ["F8A3652H1V"], "rxcui": ["856448", "856457", "856519", "856556", "856578"], "spl_set_id": ["25f9b9a3-7b0b-48d2-a458-c613bedc7cab"], "manufacturer_name": ["Lifestar Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70756-297-11)", "package_ndc": "70756-297-11", "marketing_start_date": "20260127"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (70756-297-51)", "package_ndc": "70756-297-51", "marketing_start_date": "20260127"}], "brand_name": "Propranolol hydrochloride", "product_id": "70756-297_f1ed91cc-9651-41e9-bc21-855bdf78e5fc", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70756-297", "generic_name": "Propranolol hydrochloride", "labeler_name": "Lifestar Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "60 mg/1"}], "application_number": "ANDA216663", "marketing_category": "ANDA", "marketing_start_date": "20260127", "listing_expiration_date": "20271231"}