ephedrine sulfate

Generic: ephedrine sulfate

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ephedrine sulfate
Generic Name ephedrine sulfate
Labeler remedyrepack inc.
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

ephedrine sulfate 50 mg/mL

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4433
Product ID 70518-4433_3c2fdd1c-235b-9ecf-e063-6394a90a37ee
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216146
Listing Expiration 2026-12-31
Marketing Start 2025-08-12

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 705184433
Hyphenated Format 70518-4433

Supplemental Identifiers

RxCUI
1116294
UNII
U6X61U5ZEG

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 ANDA216146 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 50 mg/mL
source: ndc
Packaging
  • 10 VIAL in 1 CARTON (70518-4433-0) / 1 mL in 1 VIAL (70518-4433-1)
source: ndc

Packages (1)

70518-4433-0 10 VIAL in 1 CARTON (70518-4433-0) / 1 mL in 1 VIAL (70518-4433-1)

Ingredients (1)

ephedrine sulfate (50 mg/mL)

Linked Drug Pages (1)

EPHEDRINE SULFATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "3c2fdd1c-235b-9ecf-e063-6394a90a37ee", "openfda": {"unii": ["U6X61U5ZEG"], "rxcui": ["1116294"], "spl_set_id": ["9851cc1c-f267-4e18-b1ad-923fe9cded84"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (70518-4433-0)  / 1 mL in 1 VIAL (70518-4433-1)", "package_ndc": "70518-4433-0", "marketing_start_date": "20250812"}], "brand_name": "EPHEDRINE SULFATE", "product_id": "70518-4433_3c2fdd1c-235b-9ecf-e063-6394a90a37ee", "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": "70518-4433", "generic_name": "EPHEDRINE SULFATE", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "EPHEDRINE SULFATE", "active_ingredients": [{"name": "EPHEDRINE SULFATE", "strength": "50 mg/mL"}], "application_number": "ANDA216146", "marketing_category": "ANDA", "marketing_start_date": "20250812", "listing_expiration_date": "20261231"}