NDC 72162-2364 – Ondansetron Hydrochloride
Ondansetron Hydrochloride 4 mg/1 · Tablet, Film Coated · Oral
Product NDC72162-2364
Product details
- Brand name
- Ondansetron Hydrochloride
- Generic name
- Ondansetron Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078539
- Marketed since
- July 31, 2007
- Listing expires
- December 31, 2027
- 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 72162-2364-5 | 500 TABLET, FILM COATED in 1 BOTTLE (72162-2364-5) | Jul 16, 2024 |
Other Ondansetron hydrochloride products
- 50090-3178 Ondansetron Hydrochloride 4 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-3185 Ondansetron Hydrochloride 8 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-4671 Ondansetron Hydrochloride 8 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 50090-6342 Ondansetron Hydrochloride 4 mg/1 · Tablet, Film Coated · A-S Medication Solutions
- 68084-221 Ondansetron Hydrochloride 8 mg/1 · Tablet, Film Coated · American Health Packaging
- 68084-220 Ondansetron Hydrochloride 4 mg/1 · Tablet, Film Coated · American Health Packaging
- 71610-119 Ondansetron Hydrochloride 8 mg/1 · Tablet, Film Coated · Aphena Pharma Solutions - Tennessee, LLC
- 76420-915 Ondansetron Hydrochloride 4 mg/1 · Tablet, Film Coated · Asclemed USA, Inc.
- 76420-916 Ondansetron Hydrochloride 8 mg/1 · Tablet, Film Coated · Asclemed USA, Inc.
- 76420-917 Ondansetron Hydrochloride 24 mg/1 · Tablet, Film Coated · Asclemed USA, Inc.
- 65862-189 Ondansetron Hydrochloride 24 mg/1 · Tablet, Film Coated · Aurobindo Pharma Limited
- 65862-187 Ondansetron Hydrochloride 4 mg/1 · Tablet, Film Coated · Aurobindo Pharma Limited