DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
GEMZAR
FDA Application No:
(NDA) 020509
Active Ingredient(s):
GEMCITABINE HYDROCHLORIDE
Company:
LILLY
Original Approval or Tentative Approval Date:
May 15, 1996
Chemical Type:
1 New molecular entity (NME)
Review Classification:
P Priority review drug
There are no Therapeutic Equivalents
Label Information
Approval History, Letters, Reviews and Related Documents
You can see the products in the same application. The table can be sorted by clicking the header columns.
Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
GEMZAR
GEMCITABINE HYDROCHLORIDE
EQ 200MG BASE/VIAL
INJECTABLE; INJECTION
Prescription
Yes
None
GEMZAR
GEMCITABINE HYDROCHLORIDE
EQ 1GM BASE/VIAL
INJECTABLE; INJECTION
Prescription
Yes
None
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