NDC 0615-8185 – Ondansetron hydrochloride
Ondansetron Hydrochloride 4 mg/1 · Tablet, Film Coated · Oral
Product NDC0615-8185
Product details
- Brand name
- Ondansetron hydrochloride
- Generic name
- Ondansetron hydrochloride
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076183
- Marketed since
- December 26, 2006
- Listing expires
- December 31, 2026
- 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 (5)
| Package NDC | Description | Since |
|---|---|---|
| 0615-8185-00 | 5 TABLET, FILM COATED in 1 BLISTER PACK (0615-8185-00) | Apr 22, 2024 |
| 0615-8185-05 | 15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8185-05) | Mar 24, 2020 |
| 0615-8185-10 | 10 TABLET, FILM COATED in 1 BLISTER PACK (0615-8185-10) | Nov 7, 2018 |
| 0615-8185-12 | 12 TABLET, FILM COATED in 1 BLISTER PACK (0615-8185-12) | Jan 26, 2024 |
| 0615-8185-39 | 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8185-39) | Nov 7, 2018 |
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