Ondansetron
- Product NDC
- 43063-560
- 11-digit product format
- 430630560
- Labeler code
- 43063
- Product ID
- 43063-560_a8da9b8e-dd3c-2415-e053-2a95a90ad145
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ondansetron
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA078050
- Marketing category
- ANDA
- Marketing start
- 2007-08-31
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 43063-560-02 | EA - Each | 43063-560 | 9a60260c-10c9-4915-9104-e213c1ce8a76 | 1 | 2015-03-03 |
| 43063-560-03 | EA - Each | 43063-560 | ef9a5ad0-5bdf-4226-ad47-891c5ff1838d | 1 | 2015-03-03 |
| 43063-560-04 | EA - Each | 43063-560 | 41d0b81b-b84a-4c36-afcf-ae98aea8cdfb | 1 | 2015-03-03 |
| 43063-560-05 | EA - Each | 43063-560 | bcd94782-02af-4ab2-9d77-665e5305c9bf | 1 | 2015-03-03 |
| 43063-560-06 | EA - Each | 43063-560 | 1611cdee-5906-4c02-9b25-339526489139 | 1 | 2015-03-03 |
| 43063-560-10 | EA - Each | 43063-560 | 805c0e53-3b5f-484f-b15f-b2cd298106f1 | 1 | 2015-03-03 |
| 43063-560-20 | EA - Each | 43063-560 | 73ba4497-1caa-4390-89ba-c7f1549060e4 | 1 | 2016-10-06 |