DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
TENEX
FDA Application No:
(NDA) 019032
Active Ingredient(s):
GUANFACINE HYDROCHLORIDE
Company:
DR REDDYS LABS INC
Original Approval or Tentative Approval Date:
October 27, 1986
Chemical Type:
1 New molecular entity (NME)
Review Classification:
S Standard review drug
Therapeutic Equivalents
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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
TENEX
GUANFACINE HYDROCHLORIDE
EQ 1MG BASE
TABLET; ORAL
Prescription
No
AB
TENEX
GUANFACINE HYDROCHLORIDE
EQ 2MG BASE
TABLET; ORAL
Prescription
Yes
AB
TENEX
GUANFACINE HYDROCHLORIDE
EQ 3MG BASE
TABLET; ORAL
Discontinued
No
None
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