Ephedrine Sulfate
- Product NDC
- 72572-151
- 11-digit product format
- 725720151
- Labeler code
- 72572
- Product ID
- 72572-151_854e6399-ce86-4576-8196-eb88e1941cb0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ephedrine Sulfate
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Civica, Inc.
- Application
- ANDA212932
- Marketing category
- ANDA
- Marketing start
- 2021-08-23
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72572-151-10 | 72572015110 | 1 VIAL, SINGLE-DOSE in 1 CARTON (72572-151-10) > 1 mL in 1 VIAL, SINGLE-DOSE (72572-151-01) | 2021-08-23 | 0000-00-00 | No | No | Current |