phenylephrine hydrochloride
Generic: phenylephrine hydrochloride
Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
phenylephrine hydrochloride
Generic Name
phenylephrine hydrochloride
Labeler
heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form
INJECTION
Routes
Active Ingredients
phenylephrine hydrochloride 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
23155-620
Product ID
23155-620_41aed9d2-a4e5-4503-a88d-17238683779c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209968
Listing Expiration
2026-12-31
Marketing Start
2023-02-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
23155620
Hyphenated Format
23155-620
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
ANDA209968 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 25 VIAL in 1 CARTON (23155-620-41) / 1 mL in 1 VIAL (23155-620-31)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "41aed9d2-a4e5-4503-a88d-17238683779c", "openfda": {"unii": ["04JA59TNSJ"], "rxcui": ["1666372"], "spl_set_id": ["f454c289-5a31-4bd3-86a2-1281bf1ab14b"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (23155-620-41) / 1 mL in 1 VIAL (23155-620-31)", "package_ndc": "23155-620-41", "marketing_start_date": "20230228"}], "brand_name": "phenylephrine hydrochloride", "product_id": "23155-620_41aed9d2-a4e5-4503-a88d-17238683779c", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "23155-620", "generic_name": "phenylephrine hydrochloride", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "phenylephrine hydrochloride", "active_ingredients": [{"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA209968", "marketing_category": "ANDA", "marketing_start_date": "20230228", "listing_expiration_date": "20261231"}