ONDANSETRON
- Product NDC
- 70518-0042
- 11-digit product format
- 705180042
- Labeler code
- 70518
- Product ID
- 70518-0042_97acccdf-dbd5-42ef-e053-2995a90a065b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ONDANSETRON
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077557
- Marketing category
- ANDA
- Marketing start
- 2017-06-05
- Marketing end
- 0000-00-00
- Substance
- ONDANSETRON
- Active strength
- 4 mg/1
- Pharmacologic classes
- Serotonin 3 Receptor Antagonists [MoA],Serotonin-3 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record