Package 71872-7303-1

Brand: phenylephrine hydrochloride

Generic: phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71872-7303-1
Digits Only 7187273031
Product NDC 71872-7303
Description

1 VIAL in 1 BAG (71872-7303-1) / 1 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2023-06-09
Brand phenylephrine hydrochloride
Generic phenylephrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "0930ec92-5653-078f-e063-6294a90aad02", "openfda": {"unii": ["04JA59TNSJ"], "rxcui": ["1666372"], "spl_set_id": ["0930ec92-5654-078f-e063-6294a90aad02"], "manufacturer_name": ["Medical Purhasing Solutions, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BAG (71872-7303-1)  / 1 mL in 1 VIAL", "package_ndc": "71872-7303-1", "marketing_start_date": "20230609"}], "brand_name": "Phenylephrine hydrochloride", "product_id": "71872-7303_0930ec92-5653-078f-e063-6294a90aad02", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "71872-7303", "generic_name": "Phenylephrine hydrochloride", "labeler_name": "Medical Purhasing Solutions, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenylephrine hydrochloride", "active_ingredients": [{"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA211081", "marketing_category": "ANDA", "marketing_start_date": "20200812", "listing_expiration_date": "20261231"}