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"25021-239-52" National Drug Code (NDC)
Gemcitabine 1 VIAL in 1 CARTON (25021-239-52) > 52.6 mL in 1 VIAL
(Sagent Pharmaceuticals)
NDC Code
25021-239-52
Package Description
1 VIAL in 1 CARTON (25021-239-52) > 52.6 mL in 1 VIAL
Product NDC
25021-239
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Gemcitabine
Non-Proprietary Name
Gemcitabine
Dosage Form
INJECTION, SOLUTION
Usage
INTRAVENOUS
Start Marketing Date
20190115
Marketing Category Name
ANDA
Application Number
ANDA209077
Manufacturer
Sagent Pharmaceuticals
Substance Name
GEMCITABINE HYDROCHLORIDE
Strength
38
Strength Unit
mg/mL
Pharmacy Classes
Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/25021-239-52