Ondansetron Hydrochloride 76420-0916
Product NDC
76420-0916- Manufacturer
- Asclemed Usa, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 31, 2007
- Listing Expires
- December 31, 2026
- Application
- ANDA078539
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ondansetron Hydrochloride | 8 mg/1 |
Drug Class
Serotonin 3 Receptor Antagonists [MoA]Serotonin-3 Receptor Antagonist [EPC]
Packaging Options(9)
1000 TABLET, FILM COATED in 1 BOTTLE (76420-916-00)
3 TABLET, FILM COATED in 1 BOTTLE (76420-916-03)
500 TABLET, FILM COATED in 1 BOTTLE (76420-916-05)
10 TABLET, FILM COATED in 1 BOTTLE (76420-916-10)
10 BLISTER PACK in 1 CARTON (76420-916-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK
30 TABLET, FILM COATED in 1 BOTTLE (76420-916-30)
1 BLISTER PACK in 1 CARTON (76420-916-33) / 3 TABLET, FILM COATED in 1 BLISTER PACK
60 TABLET, FILM COATED in 1 BOTTLE (76420-916-60)
90 TABLET, FILM COATED in 1 BOTTLE (76420-916-90)