Gemcitabine

Product NDC
45963-624
11-digit product format
459630624
Labeler code
45963
Product ID
45963-624_88b5e42c-b288-437a-85cc-d9031db65ac9
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Gemcitabine
Dosage form
INJECTION
Route
INTRAVENOUS
Labeler
Actavis Pharma, Inc.
Application
ANDA204549
Marketing category
ANDA
Marketing start
2016-04-12
Marketing end
2021-01-31
Substance
GEMCITABINE HYDROCHLORIDE
Active strength
38 mg/mL
Pharmacologic classes
Nucleic Acid Synthesis Inhibitors [MoA],Nucleoside Metabolic Inhibitor [EPC]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
45963-624-58ML - Milliliter45963-624953ba7f7-64a5-4596-921f-ed69d2c8940d12016-05-16