Oseltamivir Phosphate
- Product NDC
- 48792-7899
- 11-digit product format
- 487927899
- Labeler code
- 48792
- Product ID
- 48792-7899_a0123c0b-3e47-5f7b-e053-2a95a90ab2ec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- oseltamivir phosphate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Sunshine Lake Pharma Co., Ltd.
- Application
- ANDA212739
- Marketing category
- ANDA
- Marketing start
- 2020-03-05
- Marketing end
- 0000-00-00
- Substance
- OSELTAMIVIR PHOSPHATE
- Active strength
- 30 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 48792-7899-1 | 48792789901 | 1 BLISTER PACK in 1 CARTON (48792-7899-1) > 10 CAPSULE in 1 BLISTER PACK | 1 blister pack | 2020-03-05 | 0000-00-00 | No | No | Current |