phenylephrine hydrochloride
Generic: phenylephrine hydrochloride
Labeler: eugia us llcDrug Facts
Product Profile
Brand Name
phenylephrine hydrochloride
Generic Name
phenylephrine hydrochloride
Labeler
eugia us llc
Dosage Form
INJECTION
Routes
Active Ingredients
phenylephrine hydrochloride 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
55150-302
Product ID
55150-302_83623537-573d-40fc-8a40-e6beabf72c8c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210697
Listing Expiration
2026-12-31
Marketing Start
2020-11-13
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55150302
Hyphenated Format
55150-302
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
phenylephrine hydrochloride (source: ndc)
Generic Name
phenylephrine hydrochloride (source: ndc)
Application Number
ANDA210697 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (55150-302-01) / 10 mL in 1 VIAL, PHARMACY BULK PACKAGE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "83623537-573d-40fc-8a40-e6beabf72c8c", "openfda": {"upc": ["0355150301010", "0355150302017"], "unii": ["04JA59TNSJ"], "rxcui": ["1232651"], "spl_set_id": ["303bc1e6-0735-4ea1-84cd-6c1b621de0ed"], "manufacturer_name": ["Eugia US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (55150-302-01) / 10 mL in 1 VIAL, PHARMACY BULK PACKAGE", "package_ndc": "55150-302-01", "marketing_start_date": "20201113"}], "brand_name": "PHENYLEPHRINE HYDROCHLORIDE", "product_id": "55150-302_83623537-573d-40fc-8a40-e6beabf72c8c", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "55150-302", "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": "ANDA210697", "marketing_category": "ANDA", "marketing_start_date": "20201113", "listing_expiration_date": "20261231"}