Package 70518-3552-0

Brand: propranolol hydrochloride

Generic: propranolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-3552-0
Digits Only 7051835520
Product NDC 70518-3552
Product ID 70518-3552_3ab2ba29-baf5-b3d5-e063-6394a90a5b01
Description

90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3552-0)

Marketing

Marketing Status
Marketed Since 2022-10-09
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": "3ab2ba29-baf5-b3d5-e063-6394a90a5b01", "openfda": {"unii": ["F8A3652H1V"], "rxcui": ["856569"], "spl_set_id": ["414c4b69-38a1-4220-bec8-204c9a624b85"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3552-0)", "package_ndc": "70518-3552-0", "marketing_start_date": "20221009"}], "brand_name": "Propranolol Hydrochloride", "product_id": "70518-3552_3ab2ba29-baf5-b3d5-e063-6394a90a5b01", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70518-3552", "generic_name": "propranolol hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Propranolol Hydrochloride", "active_ingredients": [{"name": "PROPRANOLOL HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "ANDA212026", "marketing_category": "ANDA", "marketing_start_date": "20221009", "listing_expiration_date": "20261231"}