NDC 25021-235 – Gemcitabine

Gemcitabine Hydrochloride 1 g/25mL · Injection, Powder, Lyophilized, For Solution · Intravenous

Human Prescription Drug

Product NDC25021-235

Product details

Brand name
Gemcitabine
Generic name
Gemcitabine hydrochloride
Labeler
Sagent Pharmaceuticals
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Marketing category
ANDA · ANDA202485
Marketed since
December 29, 2014
Listing expires
December 31, 2027
Pharmacologic class
Nucleoside Metabolic Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Gemcitabine →

Package NDC codes (2)

Package NDCDescriptionSince
25021-235-501 VIAL in 1 CARTON (25021-235-50) / 25 mL in 1 VIALDec 29, 2014
25021-235-5110 VIAL in 1 CARTON (25021-235-51) / 25 mL in 1 VIALDec 15, 2022

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