phenylephrine hydrochloride
Generic: phenylephrine hydrochloride
Labeler: hainan poly pharm. co., ltd.Drug Facts
Product Profile
Brand Name
phenylephrine hydrochloride
Generic Name
phenylephrine hydrochloride
Labeler
hainan poly pharm. co., ltd.
Dosage Form
INJECTION
Routes
Active Ingredients
phenylephrine hydrochloride 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
14335-442
Product ID
14335-442_13fdb0eb-d8cb-ffd6-e063-6394a90a45ba
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA218412
Listing Expiration
2026-12-31
Marketing Start
2024-03-19
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
14335442
Hyphenated Format
14335-442
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
ANDA218412 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (14335-442-01) / 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": "13fdb0eb-d8cb-ffd6-e063-6394a90a45ba", "openfda": {"upc": ["0314335442108", "0314335441019", "0314335440012", "0314335442016"], "unii": ["04JA59TNSJ"], "rxcui": ["1232651", "1666372"], "spl_set_id": ["8d6973c4-4a69-4d49-9da7-d2a00df83ecb"], "manufacturer_name": ["Hainan Poly Pharm. Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (14335-442-01) / 10 mL in 1 VIAL, PHARMACY BULK PACKAGE", "package_ndc": "14335-442-01", "marketing_start_date": "20240319"}], "brand_name": "Phenylephrine Hydrochloride", "product_id": "14335-442_13fdb0eb-d8cb-ffd6-e063-6394a90a45ba", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "14335-442", "generic_name": "Phenylephrine Hydrochloride", "labeler_name": "Hainan Poly Pharm. Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenylephrine Hydrochloride", "active_ingredients": [{"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA218412", "marketing_category": "ANDA", "marketing_start_date": "20240319", "listing_expiration_date": "20261231"}