Ephedrine Sulfate
- Product NDC
- 17478-955
- 11-digit product format
- 174780955
- Labeler code
- 17478
- Product ID
- 17478-955_0e8aeb8f-1bbc-4db1-bfed-f33e546d5c19
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ephedrine Sulfate
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Akorn
- Application
- NDA208609
- Marketing category
- NDA
- Marketing start
- 2017-10-26
- Marketing end
- 0000-00-00
- Substance
- EPHEDRINE SULFATE
- Active strength
- 50 mg/mL
- Pharmacologic 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]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17478-955-10 | 17478095510 | 10 AMPULE in 1 CARTON (17478-955-10) > 1 mL in 1 AMPULE | 10 ampule | 2017-10-26 | 0000-00-00 | No | No | Current |