Tamiflu
- Product NDC
- 50090-0662
- 11-digit product format
- 500900662
- Labeler code
- 50090
- Product ID
- 50090-0662_40112622-f4e9-440b-b005-8a5a0d1d7e29
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- oseltamivir phosphate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- NDA021087
- Marketing category
- NDA
- Marketing start
- 1999-10-27
- Marketing end
- 0000-00-00
- Substance
- OSELTAMIVIR PHOSPHATE
- Active strength
- 75 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-0662-0 | 50090066200 | 1 BLISTER PACK in 1 CARTON (50090-0662-0) > 10 CAPSULE in 1 BLISTER PACK | 1 blister pack | 2014-11-28 | 0000-00-00 | No | No | Current |