68001-0282 Gemcitabine Hydrochloride

Product NDC:

68001-0282

Brand Name:

Gemcitabine Hydrochloride

Generic Name:

Gemcitabine Hydrochloride

Dosage Form Name:

INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Administration Route:

Intravenous

Substances:

Name: Gemcitabine Hydrochloride

Strength: 38.0

Unit: mg/mL

Packages:

Code: 68001-0282-22

Description:

Effective Date: July 25, 2011

Discontinued: Aug. 1, 2021

Code: 68001-0282-25

Description: 1 VIAL in 1 CARTON (68001-282-25) > 5 mL in 1 VIAL (68001-282-22)

Effective Date: May 23, 2016

Discontinued: Aug. 1, 2021

Code: 68001-0282-26

Description: 1 VIAL in 1 CARTON (68001-282-26) > 25 mL in 1 VIAL (68001-282-23)

Effective Date: May 23, 2016

Discontinued: Aug. 1, 2021

Code: 68001-0282-27

Description: 1 VIAL in 1 CARTON (68001-282-27) > 50 mL in 1 VIAL (68001-282-24)

Effective Date: May 23, 2016

Discontinued: Aug. 1, 2021

SEER*Rx Category:

Chemotherapy

Major Class:

Antimetabolite

Minor Class:

Pyrimidine Analog

Orphan Drug Designation:

Status:

No Longer Used

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