ONDANSETRON
- Product NDC
- 70518-0235
- 11-digit product format
- 705180235
- Labeler code
- 70518
- Product ID
- 70518-0235_f2143778-2cb6-70cf-e053-2995a90afba8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ONDANSETRON
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077557
- Marketing category
- ANDA
- Marketing start
- 2017-02-17
- Marketing end
- 0000-00-00
- Substance
- ONDANSETRON
- Active strength
- 8 mg/1
- Pharmacologic classes
- Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0235-0 | 70518023500 | 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (70518-0235-0) | 2017-02-17 | 0000-00-00 | No | No | Current |