Package 57631-018-00

Brand: phenylephrine hydrochloride

Generic: phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 57631-018-00
Digits Only 5763101800
Product NDC 57631-018
Description

30000 TABLET in 1 DRUM (57631-018-00)

Marketing

Marketing Status
Marketed Since 2021-01-13
Brand phenylephrine hydrochloride
Generic phenylephrine hydrochloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4024f888-60d7-f820-e063-6394a90ab81d", "openfda": {"unii": ["04JA59TNSJ"], "rxcui": ["1049182"], "spl_set_id": ["b8d360fa-0d80-f6a8-e053-2a95a90a8bd4"], "manufacturer_name": ["InvaTech Pharma Solutions LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30000 TABLET in 1 DRUM (57631-018-00)", "package_ndc": "57631-018-00", "marketing_start_date": "20210113"}], "brand_name": "Phenylephrine Hydrochloride", "product_id": "57631-018_4024f888-60d7-f820-e063-6394a90ab81d", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "57631-018", "generic_name": "Phenylephrine Hydrochloride", "labeler_name": "InvaTech Pharma Solutions 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": "20210113", "listing_expiration_date": "20261231"}