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#