Ondansetron
- Product NDC
- 72266-124
- 11-digit product format
- 722660124
- Labeler code
- 72266
- Product ID
- 72266-124_3f2b4281-55ef-43e3-e063-6294a90a56ba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ondansetron
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Fosun Pharma USA Inc.
- Application
- ANDA090648
- Marketing category
- ANDA
- Marketing start
- 2019-04-02
- Substance
- ONDANSETRON HYDROCHLORIDE
- Active strength
- 2 mg/mL
- Pharmacologic classes
- Serotonin 3 Receptor Antagonists [MoA], Serotonin-3 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Ondansetron
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ONDANSETRON HYDROCHLORIDE | 2 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | NMH84OZK2B |
| Rxcui | 283504, 1740467 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72266-124-01 | Ondansetron | 20 mL in 1 VIAL | INJECTION | 20 | | 7 |
| 72266-124-01 | Ondansetron | 1 in 1 CARTON | INJECTION | 1 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72266-124 | ONDANSETRON INJECTION [FOSUN PHARMA USA INC.] | 6 | Current NDC, Legacy NDC, 2 package rows | 20240510_e3f22b7e-b6ad-4799-93c7-d30540cada85.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 |
|---|
| 72266-124-01 | 72266012401 | 1 VIAL in 1 CARTON (72266-124-01) / 20 mL in 1 VIAL | 1 vial | 2019-04-02 | 0000-00-00 | No | No | Current |