Package 84549-621-25

Brand: phenylephrine hydrochloride

Generic: phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 84549-621-25
Digits Only 8454962125
Product NDC 84549-621
Product ID 84549-621_463d1c23-2403-026d-e063-6394a90a3bf4
Description

1 mL in 1 VIAL (84549-621-25)

Marketing

Marketing Status
Marketed Since 2025-08-27
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": ["INTRAVENOUS"], "spl_id": "463d1c23-2403-026d-e063-6394a90a3bf4", "openfda": {"unii": ["04JA59TNSJ"], "rxcui": ["1666372"], "spl_set_id": ["386663e8-f1f6-cf14-e063-6394a90a68df"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL (84549-621-25)", "package_ndc": "84549-621-25", "marketing_start_date": "20250827"}], "brand_name": "Phenylephrine hydrochloride", "product_id": "84549-621_463d1c23-2403-026d-e063-6394a90a3bf4", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "84549-621", "generic_name": "phenylephrine hydrochloride", "labeler_name": "ProPharma Distribution", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenylephrine hydrochloride", "active_ingredients": [{"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA217069", "marketing_category": "ANDA", "marketing_start_date": "20220831", "listing_expiration_date": "20261231"}