Ephedrine Sulfate
- Product NDC
- 71872-7276
- 11-digit product format
- 718727276
- Labeler code
- 71872
- Product ID
- 71872-7276_facd3e27-25dd-55ab-e053-6394a90aa8de
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ephedrine Sulfate
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA214579
- Marketing category
- ANDA
- Marketing start
- 2021-06-14
- 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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| U6X61U5ZEG | EPHEDRINE SULFATE | 134-72-5 | EPHEDRINE SULFATE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71872-7276-1 | 71872727601 | 1 VIAL, SINGLE-DOSE in 1 BAG (71872-7276-1) / 1 mL in 1 VIAL, SINGLE-DOSE | 2022-01-05 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Ephedrine Sulfate | Medical Purchasing Solutions, LLC | 2023-05-03 | HUMAN PRESCRIPTION DRUG LABEL | 2 |