> Trialight public data. Index of pages: https://trialight.com/llms.txt
> Web page: https://trialight.com/data/asset/oseltamivir-phosphate-258395ae-7f3d-48b8-9c12-7d46cfeae884
> Record changed: 2026-10-13

# Oseltamivir phosphate

Highest phase reached

Approved

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL1200340)

Drug type

Small molecule

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL1200340)

First approval year

1999

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL1200340)

## Development status

**First approval year**

1999

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL1200340)

**Listing at source**

Listed

**Highest phase reached**

Approved

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL1200340)

## Names and chemistry

**Drug type**

Small molecule

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL1200340)

**Drug name**

Oseltamivir phosphate

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL1200340)

**Molecular weight**

410.4

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL1200340)

**Structure (SMILES)**

CCOC(=O)C1=C\[C@@H\](OC(CC)CC)\[C@H\](NC(C)=O)\[C@@H\](N)C1.O=P(O)(O)O

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL1200340)

### Brand names (6)

- ebilfumin
- Ebilfumin
- oseltamivir phosphate
- Oseltamivir phosphate
- tamiflu
- Tamiflu

### Other names (47)

- (-)-Oseltamivir phosphate
- (3R-(3.ALPHA.,4.BETA.,5.ALPHA.))-ETHYL 4-(ACETYLAMINO)-5-AMINO-3-(1-ETHYLPROPOXY)-1-CYCLOHEXENE-1-CARBOXYLATE PHOSPHATE (1:1)
- 3r 3 alpha 4 beta 5 alpha ethyl 4 acetylamino 5 amino 3 1 ethylpropoxy 1 cyclohexene 1 carboxylate phosphate 1 1
- agucort
- Agucort
- Oseltamivir (as phosphate)
- oseltamivir as phosphate
- oseltamivir phosphate
- Oseltamivir phosphate
- Oseltamivir phosphate \[EP MONOGRAPH\]
- Oseltamivir phosphate \[JAN\]
- Oseltamivir phosphate \[MART.\]
- Oseltamivir phosphate \[MI\]
- Oseltamivir phosphate \[ORANGE BOOK\]
- Oseltamivir phosphate \[USAN\]
- Oseltamivir phosphate \[USP IMPURITY\]
- Oseltamivir phosphate \[USP MONOGRAPH\]
- Oseltamivir phosphate \[USP-RS\]
- Oseltamivir phosphate \[VANDF\]
- Oseltamivir phosphate \[WHO-DD\]
- Oseltamivir phosphate \[WHO-IP\]
- oseltamivir phosphate ep monograph
- oseltamivir phosphate jan
- oseltamivir phosphate mart
- oseltamivir phosphate mi

And 22 more, listed on the interactive page.

## Identifiers

**CAS registry numbers**

- 204255-11-8

**ChEMBL ID**

CHEMBL1200340

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL1200340)

**InChIKey**

PGZUMBJQJWIWGJ-ONAKXNSWSA-N

Source: [www.ebi.ac.uk](https://www.ebi.ac.uk/chembl/explore/compound/CHEMBL1200340)

**RxNorm IDs (RxCUI)**

- 259275

**FDA ingredient codes (UNII)**

- 4A3O49NGEZ

### PubChem compound IDs (2)

- 78000
- 11154112

## Regulatory information

### United States

**Applicant**

ROCHE

**Approval date**

27 Oct 1999

**Application number**

NDA021087

### Other regulatory facts

**Patents**

0

**Designations**

1

**First in class**

No

**Fast track**

No

**Breakthrough designation**

No

**Orphan designation**

No

**Priority review**

Yes

**Orphan exclusivity**

No

**Accelerated approval**

No

**Availability**

Prescription only

## Pharmacology

### Drug classification

**Drug name stem**

\-vir

#### Administration routes

- Oral

### Mechanisms of action (2)

- **Mechanism**  
Neuraminidase inhibitor

**Action type**  
Inhibitor

**Target**  
Neuraminidase

**Protein identifier**  
P03468
- **Mechanism**  
Neuraminidase inhibitor

**Action type**  
Inhibitor

**Target**  
Neuraminidase

**Protein identifier**  
P03474

### Open Targets mechanisms

- **Mechanism**  
Neuraminidase inhibitor

**Action type**  
Inhibitor

**Target**  
Neuraminidase

### Investigated indications (3)

- **Condition**  
Virus Diseases

**Highest recorded phase**  
2

**Condition identifier**  
EFO:0000763

**Subject identifier**  
D014777
- **Condition**  
Kidney Failure, Chronic

**Highest recorded phase**  
4

**Condition identifier**  
EFO:0003884

**Subject identifier**  
D007676
- **Condition**  
Influenza, Human

**Highest recorded phase**  
4

**Condition identifier**  
EFO:0007328

**Subject identifier**  
D007251

### Open Targets indications (4)

- **Condition identifier**  
EFO\_0003884
- **Condition identifier**  
EFO\_0007328
- **Condition identifier**  
MONDO\_0005300

**Highest recorded phase**  
4
- **Condition identifier**  
MONDO\_0005812

**Highest recorded phase**  
4

### Reported adverse events (12)

- **Event**  
abnormal behaviour

**Reports**  
690

**Reporting signal score**  
1,934.97
- **Event**  
convulsion

**Reports**  
158

**Reporting signal score**

117.806
- **Event**  
delirium

**Reports**  
199

**Reporting signal score**

287.141
- **Event**  
enterocolitis haemorrhagic

**Reports**  
43

**Reporting signal score**

116.701
- **Event**  
fatigue

**Reports**  
56

**Reporting signal score**

119.781
- **Event**  
hallucination

**Reports**  
307

**Reporting signal score**

451.452
- **Event**  
influenza

**Reports**  
196

**Reporting signal score**

181.444
- **Event**  
injection site pain

**Reports**  
1

**Reporting signal score**

86.5281
- **Event**  
normal newborn

**Reports**  
331

**Reporting signal score**  
1,233.88
- **Event**  
pregnancy

**Reports**  
274

**Reporting signal score**

565.467
- **Event**  
premature delivery

**Reports**  
72

**Reporting signal score**

86.0895
- **Event**  
vomiting

**Reports**  
442

**Reporting signal score**

122.371

### Trial references (11)

- NCT00803595  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT00803595)
- NCT00979251  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT00979251)
- NCT00988325  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT00988325)
- NCT01053377  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT01053377)
- NCT01053663  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT01053663)
- NCT01690637  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT01690637)
- NCT02232945  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT02232945)
- NCT02572583  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT02572583)
- NCT02662426  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT02662426)
- NCT02989012  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT02989012)
- NCT02469298  
Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT02469298)

## Dosing

**Dose**

75 mg

**Route**

Oral

**How often**

Twice daily for 5 days

## Chemical properties

**Hydrogen bond acceptors**

5

**Hydrogen bond donors**

2

**Polar surface area**

90.65

**Calculated partition coefficient (ALogP)**

1.29

**Prodrug**

Yes

**Chirality**

Single enantiomer

**Inorganic**

No

**Rule-of-five violations**

0

**Rotatable bonds**

7

**Heavy atoms**

27

**Molecular formula**

C16H31N2O8P

**Monoisotopic mass**

410.18180295

**Natural product**

No

## National Drug Codes

- 0004-0800
- 0004-0802
- 0004-0822
- 0093-8180
- 0527-4591
- 0527-4592
- 0527-4593
- 0527-5137
- 27241-139
- 31722-108
- 31722-630
- 31722-631
- 31722-632
- 33342-256
- 33342-257
- 33342-258
- 42291-567
- 42291-664
- 42291-666
- 42385-985
- 42385-986
- 42385-987
- 42677-320
- 42677-321
- 42677-322

And 101 more, listed on the interactive page.

## Evidence counts

**Recorded assays**

166

**Active assays**

20

### Active assay types

- Confirmatory

## Pharmacologic actions

- Antiviral Agents  
Agents used in the prophylaxis or therapy of VIRUS DISEASES. Some of the ways they may act include preventing viral replication by inhibiting viral DNA polymerase; binding to specific cell-surface receptors and inhibiting viral penetration or uncoating; inhibiting viral protein synthesis; or blocking late stages of virus assembly.
- Enzyme Inhibitors  
Compounds or agents that combine with an enzyme in such a manner as to prevent the normal substrate-enzyme combination and the catalytic reaction.

## Biological measurements

### Observed measurements

#### Oral bioavailability

**Median**

4.3

**Mean**

4.3

**Minimum**

4.3

**Maximum**

4.3

**Unit**

%

**Assays**

1

**Standard deviation**

0

**Summary method**

median

**Censored results excluded**

0

**Other units excluded**

0

**Unknown units excluded**

0

#### Measurement types

- F

## Related records

### Trials (138)

- A Bioequivalence Study of Oseltamivir From Oseltamivir 75 mg Caps (Pharmacare PLC, Palestine) and Tamiflu® 75 mg Caps (Hoffmann-La Roche, Switzerland)
- A Clinical Study of Treating Influenza With Liugan Shuangjie Heji
- A Clinical Trial Comparing Oseltamivir With Placebo And Zanamivir With Control As First Line Treatment For Human Swine Influenza Infection
- A Clinical Trial to Investigate the Influence of CES1 Polymorphism on Oseltamivir
- A Drug-Drug Interaction Study to Evaluate the Effect of AL-794 on the Pharmacokinetics of Oseltamivir and JNJ-63623872
- A Multicenter Randomized Open-label Study of Oseltamivir Combined With HD-DEX Versus HD-DEX in the Management of ITP
- A Multinational Phase III Study of CS-8958 (MARVEL)
- A Multiple-Dose Study of Oral Oseltamivir in Participants on Hemodialysis (HD) and Continuous Ambulatory Peritoneal Dialysis (CAPD)
- A Pharmacokinetic Study on Co-administration of Tamiflu (Oseltamivir) and Rimantadine in Healthy Volunteers
- A Pharmacokinetic/Pharmacodynamic (PK/PD) and Safety Evaluation of Oseltamivir \[Tamiflu\] in the Treatment of Infants 0 to <12 Months of Age With Confirmed Flu Infection
- A Pharmacokinetic/Pharmacodynamic Study of Oseltamivir in Immunocompromised Children With Confirmed Influenza Infection
- A Pharmacokinetics Study of Favipiravir in Patients With Severe Influenza
- A Pharmacokinetics, Pharmacodynamics and Safety Study of Warfarin in Combination With Tamiflu (Oseltamivir)
- A Phase 2 Trial Comparing Antiviral Treatments in Early Symptomatic Influenza
- A Phase 2a to Evaluate the Safety of MEDI8852 in Adults With Uncomplicated Influenza
- A Prospective/Retrospective,Randomized Controlled Clinical Study of Antiviral Therapy in the 2019-nCoV Pneumonia
- A Randomised Controlled Trial on the Effect of Post-exposure Oseltamivir Prophylaxis on Influenza Transmission in Nursing Homes
- A Randomized,Open,Controlled Clinical Study to Evaluate the Efficacy of ASC09F and Ritonavir for 2019-nCoV Pneumonia
- A Single Dose Study of Tamiflu in Volunteers in Dialysis And in Volunteers With Reduced Creatinine Clearance
- A Study of Intravenous Oseltamivir \[Tamiflu\] in Infants With Influenza

### Approved for (2)

- [Chronic kidney disease](https://trialight.com/data/condition/chronic-kidney-disease-dc1fecbb-338b-5bbc-8d68-08e49db49918.md)
- [Influenza](https://trialight.com/data/condition/influenza-ea12369b-7ed6-5f6b-94fe-eb0e56c24def.md)

### In development for (1)

- [Viral infectious disease](https://trialight.com/data/condition/viral-infectious-disease-43db42a3-adad-5b9d-b74c-f17df0674c21.md) Phase 2

---

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