ephedrine sulfate

Generic: ephedrine sulfate

Labeler: endo usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name ephedrine sulfate
Generic Name ephedrine sulfate
Labeler endo usa, inc.
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

ephedrine sulfate 5 mg/mL

Manufacturer
Endo USA, Inc.

Identifiers & Regulatory

Product NDC 42023-243
Product ID 42023-243_b8d2389a-6624-4a8e-bd12-4f62334d7335
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA213994
Listing Expiration 2026-12-31
Marketing Start 2024-01-31

Pharmacologic Class

Classes
adrenergic alpha-agonists [moa] adrenergic beta-agonists [moa] increased norepinephrine activity [pe] norepinephrine releasing agent [epc] alpha-adrenergic agonist [epc] beta-adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42023243
Hyphenated Format 42023-243

Supplemental Identifiers

RxCUI
2368456
UNII
U6X61U5ZEG

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 ephedrine sulfate (source: ndc)
Generic Name ephedrine sulfate (source: ndc)
Application Number NDA213994 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 5 mg/mL
source: ndc
Packaging
  • 10 mL in 1 VIAL, SINGLE-DOSE (42023-243-99)
source: ndc

Packages (1)

42023-243-99 10 mL in 1 VIAL, SINGLE-DOSE (42023-243-99)

Ingredients (1)

ephedrine sulfate (5 mg/mL)

Linked Drug Pages (2)

EPHEDRINE SULFATE ndc-match (0.9) EPHEDRINE SULFATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "b8d2389a-6624-4a8e-bd12-4f62334d7335", "openfda": {"unii": ["U6X61U5ZEG"], "rxcui": ["2368456"], "spl_set_id": ["a247857e-ba7b-4a37-b132-4ba9b0d1c4d1"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 mL in 1 VIAL, SINGLE-DOSE (42023-243-99)", "package_ndc": "42023-243-99", "marketing_start_date": "20240131"}], "brand_name": "EPHEDRINE SULFATE", "product_id": "42023-243_b8d2389a-6624-4a8e-bd12-4f62334d7335", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Adrenergic beta-Agonists [MoA]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Releasing Agent [EPC]", "alpha-Adrenergic Agonist [EPC]", "beta-Adrenergic Agonist [EPC]"], "product_ndc": "42023-243", "generic_name": "Ephedrine Sulfate", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "EPHEDRINE SULFATE", "active_ingredients": [{"name": "EPHEDRINE SULFATE", "strength": "5 mg/mL"}], "application_number": "NDA213994", "marketing_category": "NDA", "marketing_start_date": "20240131", "listing_expiration_date": "20261231"}