Ephedrine Sulfate

Product NDC
14789-014
11-digit product format
147890014
Labeler code
14789
Product ID
14789-014_d483665c-4eaf-495f-94ed-c155f5d45f1c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ephedrine Sulfate
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Labeler
Nexus Pharmaceuticals Inc
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2015-06-08
Marketing end
0000-00-00
Substance
EPHEDRINE SULFATE
Active strength
50 mg/mL
Pharmacologic classes
alpha-Adrenergic Agonist [EPC],Adrenergic alpha-Agonists [MoA],beta-Adrenergic Agonist [EPC],Adrenergic beta-Agonists [MoA],Norepinephrine Releasing Agent [EPC],Increased Norepinephrine Activity [PE]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
14789-014-012023-09-26C16284748780-19d75b9d0-d14d-f424-e053-dadaa90a57ce16f212c3-d504-4d3c-813e-cc23a04aaa88
14789-014-012020-01-31C16284748780-19d75b9d0-d14d-f424-e053-dadaa90a57ce16f212c3-d504-4d3c-813e-cc23a04aaa88

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
14789-014-01ML - Milliliter14789-014f8dd1d7a-33eb-4c68-9271-4984eeea19e312015-09-10