Package 83586-010-00

Brand: phenylephrine hydrochloride

Generic: phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 83586-010-00
Digits Only 8358601000
Product NDC 83586-010
Product ID 83586-010_3e763082-1ab4-0eeb-e063-6394a90af78b
Description

130000 TABLET in 1 DRUM (83586-010-00)

Marketing

Marketing Status
Marketed Since 2025-09-10
Brand phenylephrine hydrochloride
Generic phenylephrine hydrochloride
Sample Package No

Linked Drug Pages (1)

PHENYLEPHRINE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3e763082-1ab4-0eeb-e063-6394a90af78b", "openfda": {"unii": ["04JA59TNSJ"], "rxcui": ["1049182"], "spl_set_id": ["5d8b980f-0011-41e3-a881-ad10fe399079"], "manufacturer_name": ["HHH PHARMA USA LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "130000 TABLET in 1 DRUM (83586-010-00)", "package_ndc": "83586-010-00", "marketing_start_date": "20250910"}], "brand_name": "PHENYLEPHRINE HYDROCHLORIDE", "product_id": "83586-010_3e763082-1ab4-0eeb-e063-6394a90af78b", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "83586-010", "generic_name": "PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "HHH PHARMA USA LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "PHENYLEPHRINE HYDROCHLORIDE", "active_ingredients": [{"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250910", "listing_expiration_date": "20261231"}