Sumansetron
- Product NDC
- 59088-772
- 11-digit product format
- 590880772
- Labeler code
- 59088
- Product ID
- 59088-772_f2054b5e-a881-1bd5-e053-2a95a90a015c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- sumatriptan succinate, ondansetron
- Dosage form
- KIT
- Labeler
- PureTek Corporation
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2021-01-01
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sumansetron
- Listing expiration
- 2026-12-31
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Rxcui | 198052, 313161 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59088-772-00 | Sumansetron | 1 in 1 PACKAGE | KIT | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59088-772 | SUMANSETRON (SUMATRIPTAN SUCCINATE, ONDANSETRON) KIT [PURETEK CORPORATION] | 2 | Current NDC, Legacy NDC, 1 package rows | 20230112_b69f0762-a2f7-28c7-e053-2995a90a0484.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59088-772-00 | 59088077200 | 1 KIT in 1 PACKAGE (59088-772-00) * 9 BLISTER PACK in 1 CARTON (55111-292-09) / 9 TABLET in 1 BLISTER PACK * 30 TABLET, FILM COATED in 1 BOTTLE (45963-538-30) | 1 kit | 2021-01-01 | 0000-00-00 | No | No | Current |