NDC 0143-9342 – Gemcitabine
Gemcitabine Hydrochloride 38 mg/mL · Injection, Solution · Intravenous
Product NDC0143-9342
Product details
- Brand name
- Gemcitabine
- Generic name
- Gemcitabine
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Dosage form
- Injection, Solution
- Route
- Intravenous
- Marketing category
- ANDA · ANDA213175
- Marketed since
- October 17, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nucleoside Metabolic Inhibitor
Active ingredients
- Gemcitabine Hydrochloride 38 mg/mL
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0143-9342-01 | 1 VIAL in 1 CARTON (0143-9342-01) / 52.6 mL in 1 VIAL | Oct 17, 2025 |
Recalls mentioning this NDC
- D-0714-2026 Jul 8, 2026 · Class II
Temperature Abuse: Product was stored incorrectly in a controlled room temperature environment instead of a refrigerated environment.
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