Package 70518-1463-0

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-1463-0
Digits Only 7051814630
Product NDC 70518-1463
Product ID 70518-1463_4900c8ab-3b55-e02c-e063-6394a90ace9e
Description

90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-1463-0)

Marketing

Marketing Status
Marketed Since 2018-10-04
Brand propranolol hydrochloride
Generic propranolol hydrochloride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4900c8ab-3b55-e02c-e063-6394a90ace9e", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856460"], "spl_set_id": ["e0241448-5727-4c68-ae2a-6f41cd962d7c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-1463-0)", "package_ndc": "70518-1463-0", "marketing_start_date": "20181004"}], "brand_name": "propranolol hydrochloride", "product_id": "70518-1463_4900c8ab-3b55-e02c-e063-6394a90ace9e", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-1463", "generic_name": "propranolol hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "propranolol hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA078703", "marketing_category": "ANDA", "marketing_start_date": "20181004", "listing_expiration_date": "20271231"}