NDC 60760-636 – Ondansetron Hydrochloride
Ondansetron Hydrochloride 4 mg/1 · Tablet, Film Coated · Oral
Product NDC60760-636
Product details
- Brand name
- Ondansetron Hydrochloride
- Generic name
- Ondansetron Hydrochloride
- Labeler
- St. Mary's Medical Park Pharmacy
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 60760-636-10 | 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-636-10) | Jul 31, 2007 |
| 60760-636-16 | 16 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-636-16) | Mar 3, 2023 |
| 60760-636-20 | 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-636-20) | Mar 26, 2018 |
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