phenylephrine hydrochloride
Generic: phenylephrine hydrochloride
Labeler: meitheal pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
phenylephrine hydrochloride
Generic Name
phenylephrine hydrochloride
Labeler
meitheal pharmaceuticals inc.
Dosage Form
INJECTION
Routes
Active Ingredients
phenylephrine hydrochloride 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
71288-807
Product ID
71288-807_8c63c2aa-de67-4214-99bc-ba483b08d2b5
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210334
Listing Expiration
2026-12-31
Marketing Start
2018-04-27
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71288807
Hyphenated Format
71288-807
Supplemental Identifiers
RxCUI
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
ANDA210334 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 25 VIAL, SINGLE-DOSE in 1 CARTON (71288-807-02) / 1 mL in 1 VIAL, SINGLE-DOSE (71288-807-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "8c63c2aa-de67-4214-99bc-ba483b08d2b5", "openfda": {"unii": ["04JA59TNSJ"], "rxcui": ["1666372"], "spl_set_id": ["f2096e12-cbeb-4084-9132-17c7ef46b7b9"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (71288-807-02) / 1 mL in 1 VIAL, SINGLE-DOSE (71288-807-01)", "package_ndc": "71288-807-02", "marketing_start_date": "20180427"}], "brand_name": "PHENYLEPHRINE HYDROCHLORIDE", "product_id": "71288-807_8c63c2aa-de67-4214-99bc-ba483b08d2b5", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "71288-807", "generic_name": "PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "Meitheal Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PHENYLEPHRINE HYDROCHLORIDE", "active_ingredients": [{"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA210334", "marketing_category": "ANDA", "marketing_start_date": "20180427", "listing_expiration_date": "20261231"}