NDC 55700-631 – Ondansetron Hydrochloride
Ondansetron Hydrochloride 4 mg/1 · Tablet, Film Coated · Oral
Product NDC55700-631
Product details
- Brand name
- Ondansetron Hydrochloride
- Generic name
- Ondansetron Hydrochloride
- Labeler
- Quality Care Products LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078539
- Marketed since
- May 25, 2018
- Marketing end
- January 31, 2028
- Pharmacologic class
- Serotonin-3 Receptor Antagonist
Active ingredients
- Ondansetron Hydrochloride 4 mg/1
Uses, dosage, side effects and warnings for Ondansetron hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 55700-631-10 | 10 TABLET, FILM COATED in 1 BOTTLE (55700-631-10) | May 25, 2018 |
| 55700-631-20 | 20 TABLET, FILM COATED in 1 BOTTLE (55700-631-20) | May 25, 2018 |
| 55700-631-30 | 30 TABLET, FILM COATED in 1 BOTTLE (55700-631-30) | May 25, 2018 |
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