NDC 25021-239 – Gemcitabine
Gemcitabine Hydrochloride 38 mg/mL · Injection, Solution · Intravenous
Product NDC25021-239
Product details
- Brand name
- Gemcitabine
- Generic name
- Gemcitabine
- Labeler
- Sagent Pharmaceuticals
- Dosage form
- Injection, Solution
- Route
- Intravenous
- Marketing category
- ANDA · ANDA209077
- Marketed since
- January 15, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nucleoside Metabolic Inhibitor
Active ingredients
- Gemcitabine Hydrochloride 38 mg/mL
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 25021-239-05 | 1 VIAL in 1 CARTON (25021-239-05) / 5.26 mL in 1 VIAL | Jan 15, 2019 |
| 25021-239-26 | 1 VIAL in 1 CARTON (25021-239-26) / 26.3 mL in 1 VIAL | Jan 15, 2019 |
| 25021-239-52 | 1 VIAL in 1 CARTON (25021-239-52) / 52.6 mL in 1 VIAL | Jan 15, 2019 |
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