DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
OCTREOTIDE ACETATE
FDA Application No:
(ANDA) 077373
Active Ingredient(s):
OCTREOTIDE ACETATE
Company:
SUN PHARM INDS
Original Approval or Tentative Approval Date:
August 14, 2007
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
OCTREOTIDE ACETATE
OCTREOTIDE ACETATE
EQ 0.2MG BASE/ML
INJECTABLE; INJECTION
Prescription
No
AP
OCTREOTIDE ACETATE
OCTREOTIDE ACETATE
EQ 1MG BASE/ML
INJECTABLE; INJECTION
Prescription
No
AP
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