Tamiflu
- Product NDC
- 70518-2042
- 11-digit product format
- 705182042
- Labeler code
- 70518
- Product ID
- 70518-2042_daf6f6a3-3e30-cff5-e053-2a95a90a2635
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- oseltamivir phosphate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA021087
- Marketing category
- NDA
- Marketing start
- 2019-04-26
- Marketing end
- 0000-00-00
- Substance
- OSELTAMIVIR PHOSPHATE
- Active strength
- 75 mg/1
- Pharmacologic classes
- Neuraminidase Inhibitor [EPC], Neuraminidase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2042-0 | 70518204200 | 1 BLISTER PACK in 1 CARTON (70518-2042-0) > 10 CAPSULE in 1 BLISTER PACK | 1 blister pack | 2019-04-26 | 0000-00-00 | No | No | Current |