ephedrine sulfate
Generic: ephedrine sulfate
Labeler: par health usa, llcDrug Facts
Product Profile
Brand Name
ephedrine sulfate
Generic Name
ephedrine sulfate
Labeler
par health usa, llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
ephedrine sulfate 50 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
42023-216
Product ID
42023-216_866144c4-9b6c-49c8-b165-a8775265efcd
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA208943
Listing Expiration
2026-12-31
Marketing Start
2017-02-16
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
42023216
Hyphenated Format
42023-216
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
ephedrine sulfate (source: ndc)
Generic Name
ephedrine sulfate (source: ndc)
Application Number
NDA208943 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/mL
Packaging
- 25 VIAL in 1 CARTON (42023-216-25) / 1 mL in 1 VIAL (42023-216-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "866144c4-9b6c-49c8-b165-a8775265efcd", "openfda": {"unii": ["U6X61U5ZEG"], "rxcui": ["1116294"], "spl_set_id": ["38723cb3-dfca-4c81-8c6f-63dd99929191"], "manufacturer_name": ["Par Health USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (42023-216-25) / 1 mL in 1 VIAL (42023-216-01)", "package_ndc": "42023-216-25", "marketing_start_date": "20170216"}], "brand_name": "Ephedrine Sulfate", "product_id": "42023-216_866144c4-9b6c-49c8-b165-a8775265efcd", "dosage_form": "INJECTION, SOLUTION", "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": "42023-216", "generic_name": "Ephedrine Sulfate", "labeler_name": "Par Health USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ephedrine Sulfate", "active_ingredients": [{"name": "EPHEDRINE SULFATE", "strength": "50 mg/mL"}], "application_number": "NDA208943", "marketing_category": "NDA", "marketing_start_date": "20170216", "listing_expiration_date": "20261231"}