Drugs@FDA: FDA-Approved Drugs
Abbreviated New Drug Application (ANDA): 218211
Company: GLAND
Company: GLAND
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
|---|---|---|---|---|---|---|---|
| EPHEDRINE SULFATE | EPHEDRINE SULFATE | 50MG/10ML (5MG/ML) | SOLUTION;INTRAVENOUS | Prescription | AP1 | No | No |
Original Approvals or Tentative Approvals
| Action Date | Submission | Action Type | Submission Classification | Review Priority; Orphan Status | Letters, Reviews, Labels, Patient Package Insert | Notes | Url |
|---|---|---|---|---|---|---|---|
| 01/16/2025 | ORIG-1 | Approval | STANDARD |
Letter (PDF)
|
Label is not available on this site. |
https://www.accessdata.fda.gov/drugsatfda_docs/appletter/2025/218211Orig1s000ltr.pdf |
EPHEDRINE SULFATE
SOLUTION;INTRAVENOUS; 50MG/10ML (5MG/ML)
TE Code = AP1
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | RLD | TE Code | Application No. | Company |
|---|---|---|---|---|---|---|---|---|
| EMERPHED | EPHEDRINE SULFATE | 50MG/10ML (5MG/ML) | SOLUTION;INTRAVENOUS | Prescription | Yes | AP1 | 213407 | NEXUS |
| EPHEDRINE SULFATE | EPHEDRINE SULFATE | 50MG/10ML (5MG/ML) | SOLUTION;INTRAVENOUS | Prescription | No | AP1 | 218211 | GLAND |