NDC 0143-9701 – Irinotecan Hydrochloride
Irinotecan Hydrochloride 20 mg/mL · Injection · Intravenous
Product NDC0143-9701
Product details
- Brand name
- Irinotecan Hydrochloride
- Generic name
- Irinotecan Hydrochloride
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Dosage form
- Injection
- Route
- Intravenous
- Marketing category
- ANDA · ANDA091032
- Marketed since
- December 20, 2010
- Listing expires
- December 31, 2026
- Pharmacologic class
- Topoisomerase Inhibitor
Active ingredients
- Irinotecan Hydrochloride 20 mg/mL
Uses, dosage, side effects and warnings for Irinotecan Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0143-9701-01 | 5 mL in 1 VIAL, GLASS (0143-9701-01) | Dec 20, 2010 |
Recalls mentioning this NDC
- D-1308-2020 Jun 24, 2020 · Class II
Defective Container: Customer complaints received of a crimp defect while removing the flip-cap during use. - D-66447-002 Nov 13, 2013 · Class II
Superpotent Drug: a recent review of the USP revealed that an incorrect calculation was used to determine the amount of irinotecan to use in formulation which will result in an assay higher than the… - D-66447-001 Nov 13, 2013 · Class II
Superpotent Drug: a recent review of the USP revealed that an incorrect calculation was used to determine the amount of irinotecan to use in formulation which will result in an assay higher than the…
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