DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
CEENU
FDA Application No:
(NDA) 017588
Active Ingredient(s):
LOMUSTINE
Company:
BRISTOL MYERS SQUIBB
Original Approval or Tentative Approval Date:
August 4, 1976
Chemical Type:
1 New molecular entity (NME)
Review Classification:
S Standard review drug
There are no Therapeutic Equivalents
Labels are not available
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
CEENU
LOMUSTINE
10MG
CAPSULE; ORAL
Prescription
No
None
CEENU
LOMUSTINE
40MG
CAPSULE; ORAL
Prescription
No
None
CEENU
LOMUSTINE
100MG
CAPSULE; ORAL
Prescription
Yes
None
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