Package 55150-300-25

Brand: phenylephrine hydrochloride

Generic: phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 55150-300-25
Digits Only 5515030025
Product NDC 55150-300
Description

25 VIAL, SINGLE-DOSE in 1 CARTON (55150-300-25) / 1 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2021-01-07
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": "a816de08-7a48-43df-a09b-f1f342a230d5", "openfda": {"unii": ["04JA59TNSJ"], "rxcui": ["1666372"], "spl_set_id": ["c2ba1b3e-94bc-494d-b0fe-4ab9dd61dddc"], "manufacturer_name": ["Eugia US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (55150-300-25)  / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "55150-300-25", "marketing_start_date": "20210107"}], "brand_name": "Phenylephrine Hydrochloride", "product_id": "55150-300_a816de08-7a48-43df-a09b-f1f342a230d5", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "55150-300", "generic_name": "Phenylephrine Hydrochloride", "labeler_name": "Eugia US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenylephrine Hydrochloride", "active_ingredients": [{"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA210696", "marketing_category": "ANDA", "marketing_start_date": "20210107", "listing_expiration_date": "20271231"}