phenylephrine hydrochloride

Generic: phenylephrine hydrochloride

Labeler: novadoz pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name phenylephrine hydrochloride
Generic Name phenylephrine hydrochloride
Labeler novadoz pharmaceuticals llc
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

phenylephrine hydrochloride 10 mg/mL

Manufacturer
Novadoz Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 72205-266
Product ID 72205-266_0bb7af81-62ec-4ae7-8055-89453f7a161d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA217521
Listing Expiration 2026-12-31
Marketing Start 2023-07-10

Pharmacologic Class

Classes
adrenergic alpha1-agonists [moa] alpha-1 adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72205266
Hyphenated Format 72205-266

Supplemental Identifiers

RxCUI
1232651 1666372
UPC
0372205266070 0372205265073 0372205265011 0372205266018
UNII
04JA59TNSJ

Packaging Origin

Original Packager
true

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 ANDA217521 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 10 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (72205-266-07) / 10 mL in 1 VIAL, PHARMACY BULK PACKAGE (72205-266-01)
source: ndc

Packages (1)

72205-266-07 10 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (72205-266-07) / 10 mL in 1 VIAL, PHARMACY BULK PACKAGE (72205-266-01)

Ingredients (1)

phenylephrine hydrochloride (10 mg/mL)

Linked Drug Pages (1)

PHENYLEPHRINE HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "0bb7af81-62ec-4ae7-8055-89453f7a161d", "openfda": {"upc": ["0372205266070", "0372205265073", "0372205265011", "0372205266018"], "unii": ["04JA59TNSJ"], "rxcui": ["1232651", "1666372"], "spl_set_id": ["0bb7af81-62ec-4ae7-8055-89453f7a161d"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (72205-266-07)  / 10 mL in 1 VIAL, PHARMACY BULK PACKAGE (72205-266-01)", "package_ndc": "72205-266-07", "marketing_start_date": "20240504"}], "brand_name": "PHENYLEPHRINE HYDROCHLORIDE", "product_id": "72205-266_0bb7af81-62ec-4ae7-8055-89453f7a161d", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "72205-266", "generic_name": "PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PHENYLEPHRINE HYDROCHLORIDE", "active_ingredients": [{"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA217521", "marketing_category": "ANDA", "marketing_start_date": "20230710", "listing_expiration_date": "20261231"}