ZONTIVITY
- Product NDC
- 66992-208
- 11-digit product format
- 669920208
- Labeler code
- 66992
- Product ID
- 66992-208_eb55583e-2701-6426-e053-2a95a90abb4f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- vorapaxar
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- WraSer Pharmaceuticals, LLC
- Application
- NDA204886
- Marketing category
- NDA
- Marketing start
- 2022-09-21
- Marketing end
- 0000-00-00
- Substance
- VORAPAXAR SULFATE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Protease-activated Receptor-1 Antagonist [EPC], Protease-activated Receptor-1 Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 66992-208-30 | ZONTIVITY | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 2 |
| 66992-208-90 | ZONTIVITY | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 66992-208 | ZONTIVITY (VORAPAXAR) TABLET, FILM COATED [WRASER PHARMACEUTICALS, LLC] | 2 | Legacy NDC, 2 package rows | 20221019_f2abe3ed-ed3d-4215-a489-b18341ce85bc.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 66992-208-30 | 66992020830 | 30 TABLET, FILM COATED in 1 BOTTLE (66992-208-30) | 2022-09-21 | 0000-00-00 | No | No | Current |
| 66992-208-90 | 66992020890 | 90 TABLET, FILM COATED in 1 BOTTLE (66992-208-90) | 2022-09-21 | 0000-00-00 | No | No | Current |