Package 70518-3102-4

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3102-4
Digits Only 7051831024
Product NDC 70518-3102
Description

90 TABLET in 1 BOTTLE, PLASTIC (70518-3102-4)

Marketing

Marketing Status
Marketed Since 2025-04-16
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": "4bceaf8b-7301-9096-e063-6294a90a81cf", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856448"], "spl_set_id": ["07c3fcab-33fe-4a6a-ba67-2d042190c146"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3102-0)", "package_ndc": "70518-3102-0", "marketing_start_date": "20210526"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3102-1)", "package_ndc": "70518-3102-1", "marketing_start_date": "20220825"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-3102-3)", "package_ndc": "70518-3102-3", "marketing_start_date": "20240417"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-3102-4)", "package_ndc": "70518-3102-4", "marketing_start_date": "20250416"}], "brand_name": "Propranolol Hydrochloride", "product_id": "70518-3102_4bceaf8b-7301-9096-e063-6294a90a81cf", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-3102", "generic_name": "Propranolol Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA070322", "marketing_category": "ANDA", "marketing_start_date": "20210526", "listing_expiration_date": "20271231"}