| NDC | 70934-193-06, 70934-193-12 |
| Set ID | 86a69949-808e-5a9e-e053-2991aa0a78ea |
| Category | HUMAN PRESCRIPTION DRUG LABEL |
| Packager | Denton Pharma, Inc. DBA Northwind Pharmaceuticals |
| Generic Name | |
| Product Class | |
| Product Number | |
| Application Number | ANDA078539 |
![ONDANSETRON HYDROCHLORIDE TABLET, FILM COATED [DENTON PHARMA, INC. DBA NORTHWIND PHARMACEUTICAL]](https://medic.hrt.org//dailymed/images/3843/70934-193-12 Master Bottle Label Approval - Rev B 06-19.jpg)
![ONDANSETRON HYDROCHLORIDE TABLET, FILM COATED [DENTON PHARMA, INC. DBA NORTHWIND PHARMACEUTICAL]](https://medic.hrt.org//dailymed/images/3843/ondansetron-str.jpg)
| NDC | 70934-193-06, 70934-193-12 |
| Set ID | 86a69949-808e-5a9e-e053-2991aa0a78ea |
| Category | HUMAN PRESCRIPTION DRUG LABEL |
| Packager | Denton Pharma, Inc. DBA Northwind Pharmaceuticals |
| Generic Name | |
| Product Class | |
| Product Number | |
| Application Number | ANDA078539 |