Package 70069-591-10

Brand: phenylephrine hydrochloride

Generic: phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70069-591-10
Digits Only 7006959110
Product NDC 70069-591
Description

10 AMPULE in 1 CARTON (70069-591-10) / 5 mL in 1 AMPULE (70069-591-01)

Marketing

Marketing Status
Marketed Since 2025-03-04
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": "5bc23817-cddb-4448-bbf3-969db4cee912", "openfda": {"upc": ["0370069591017", "0370069591109"], "unii": ["04JA59TNSJ"], "rxcui": ["2262018"], "spl_set_id": ["170e63f1-23f4-4839-ab89-b81832d94a56"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 AMPULE in 1 CARTON (70069-591-10)  / 5 mL in 1 AMPULE (70069-591-01)", "package_ndc": "70069-591-10", "marketing_start_date": "20250304"}], "brand_name": "Phenylephrine Hydrochloride", "product_id": "70069-591_5bc23817-cddb-4448-bbf3-969db4cee912", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "70069-591", "generic_name": "Phenylephrine Hydrochloride", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenylephrine Hydrochloride", "active_ingredients": [{"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": ".1 mg/mL"}], "application_number": "ANDA215617", "marketing_category": "ANDA", "marketing_start_date": "20250304", "listing_expiration_date": "20261231"}