51754-4200 : Akovaz 50 mg/ml Intravenous Injection
| NDC: | 51754-4200 |
| Labeler: | Exela Pharma Sciences, LLC |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Akovaz |
| Dosage Form: | Intravenous Injection |
| Application #: | NDA208289 |
| Rev. Date: |
NDC Package Codes:
- 51754-4200-4: 25 VIAL, SINGLE‑DOSE IN 1 CARTON (51754‑4200‑4) > 1 ML IN 1 VIAL, SINGLE‑DOSE
Active Ingredients:
- Ephedrine Sulfate
Dosage Strength:
- 50 mg/mL
Pharmaceutical 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]
Related Products:
Based on records with the same trade name.- 51754-4250 Akovaz 50 mg/ml Intravenous Injection by Exela Pharma Sciences, LLC
- 68001-330 Akovaz 50 mg/ml Intravenous Injection by Bluepoint Laboratories
- 76014-005 Akovaz 50 mg/ml Intravenous Injection by éclat Pharmaceuticals, LLC
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.