Oseltamivir Phosphate
- Product NDC
- 71205-617
- 11-digit product format
- 712050617
- Labeler code
- 71205
- Product ID
- 71205-617_5d4433aa-fc83-4868-b47f-e9b8674f3b3e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oseltamivir Phosphate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA209438
- Marketing category
- ANDA
- Marketing start
- 2018-02-23
- Substance
- OSELTAMIVIR PHOSPHATE
- Active strength
- 75 mg/1
- Pharmacologic classes
- Neuraminidase Inhibitor [EPC], Neuraminidase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 4A3O49NGEZ | OSELTAMIVIR PHOSPHATE | 204255-11-8 | OSELTAMIVIR PHOSPHATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71205-617-10 | 71205061710 | 10 CAPSULE in 1 CARTON (71205-617-10) | 10 capsule | 2021-11-02 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Oseltamivir Phosphate | Proficient Rx LP | 2022-09-01 | HUMAN PRESCRIPTION DRUG LABEL | 2 |