NDC 16714-909 – Gemcitabine
Gemcitabine Hydrochloride 200 mg/1 · Injection, Powder, Lyophilized, For Solution · Intravenous
Product NDC16714-909
Product details
- Brand name
- Gemcitabine
- Generic name
- Gemcitabine Hydrochloride
- Labeler
- NorthStar Rx LLC
- Dosage form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Marketing category
- ANDA · ANDA091365
- Marketed since
- November 1, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- Nucleoside Metabolic Inhibitor
Active ingredients
- Gemcitabine Hydrochloride 200 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 16714-909-01 | 1 VIAL, SINGLE-DOSE in 1 CARTON (16714-909-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE | Nov 1, 2018 |
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