NDC 70069-819 – Ephedrine Sulfate
Ephedrine Sulfate 50 mg/mL · Injection · Intravenous
Product NDC70069-819
Product details
- Brand name
- Ephedrine Sulfate
- Generic name
- Ephedrine Sulfate
- Labeler
- Somerset Therapeutics, LLC
- Dosage form
- Injection
- Route
- Intravenous
- Marketing category
- ANDA · ANDA216146
- Marketed since
- November 7, 2024
- Listing expires
- December 31, 2026
- Pharmacologic class
- Norepinephrine Releasing Agent; alpha-Adrenergic Agonist; beta-Adrenergic Agonist
Active ingredients
- Ephedrine Sulfate 50 mg/mL
Uses, dosage, side effects and warnings for Ephedrine Sulfate →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 70069-819-10 | 10 VIAL in 1 CARTON (70069-819-10) / 1 mL in 1 VIAL | Nov 7, 2024 |
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