93 7236
Pill imprint 93 7236 has been identified as Ondansetron hydrochloride 8 mg.
Ondansetron is used in the treatment of nausea/vomiting; nausea/vomiting, chemotherapy induced; gastroenteritis; nausea/vomiting, postoperative; obsessive compulsive disorder (and more), and belongs to the drug class 5HT3 receptor antagonists. There is no proven risk in humans during pregnancy.
Ondansetron 8 mg is not subject to the Controlled Substances Act.
See also related documents.
Ondansetron hydrochloride Images
- Imprint:
-
93
7236 - Strength:
- 8 mg
- Color:
- Yellow
- Size:
- 8.00 mm
- Shape:
- Round
- Availability:
- Prescription only
- Inactive Ingredients:
- hypromelloses
lactose monohydrate
magnesium stearate
microcrystalline cellulose
corn starch
polyethylene glycol
sodium starch glycolate type A potato
titanium dioxide
ferric oxide yellow
- Drug Class:
- 5HT3 receptor antagonists
- Pregnancy Category:
- B - No proven risk in humans
- CSA Schedule:
- N - Not a controlled drug
- Manufacturer:
- Teva Pharmaceuticals USA
- National Drug Code (NDC):
- 00093-7236
| NDC Code | Manufacturer / Repackager |
|---|---|
| 35356-0445 | Lake Erie Medical and Surgical Supply (repackager) |
Note: Inactive ingredients may vary.
Advertisement
More Ondansetron Hydrochloride resources
- Ondansetron
- Ondansetron (Wolters Kluwer)
- Ondansetron Orally Disintegrating Tablets (Wolters Kluwer)
- Ondansetron Soluble Film (Wolters Kluwer)
- Ondansetron Solution (Wolters Kluwer)
- Ondansetron Tablets (Wolters Kluwer)
- ondansetron (Cerner Multum)
- ondansetron injection (Cerner Multum)
- ondansetron Oral, Injection, Intravenous (Micromedex) - Includes Dosage Information
- ondansetron Oral, Oromucosal (Micromedex) - Includes Dosage Information
- Ondansetron Hydrochloride (AHFS DI)
- Ondansetron (FDA)
- Ondansetron Injection (FDA)
- Ondansetron ODT (FDA)
- Ondansetron Oral Solution (FDA)
- Ondansetron and Dextrose (FDA)
- Zofran Injection (FDA)
- Ondansetron Hydrochloride (Wolters Kluwer)
Search Again
