DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
GEREF
FDA Application No:
(NDA) 020443
Active Ingredient(s):
SERMORELIN ACETATE
Company:
EMD SERONO
Original Approval or Tentative Approval Date:
September 26, 1997
Chemical Type:
3 New dosage form
Review Classification:
S Standard review drug
O Orphan 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
GEREF
SERMORELIN ACETATE
EQ 0.5MG BASE/VIAL
INJECTABLE; INJECTION
Discontinued
No
None
GEREF
SERMORELIN ACETATE
EQ 1MG BASE/VIAL
INJECTABLE; INJECTION
Discontinued
No
None
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