DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
OMEPRAZOLE
FDA Application No:
(ANDA) 075757
Active Ingredient(s):
OMEPRAZOLE
Company:
LEK PHARMS
Original Approval or Tentative Approval Date:
January 28, 2003
Therapeutic Equivalents
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Approval History, Letters, Reviews and Related Documents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
OMEPRAZOLE
OMEPRAZOLE
10MG
CAPSULE, DELAYED REL PELLETS; ORAL
Prescription
No
AB
OMEPRAZOLE
OMEPRAZOLE
20MG
CAPSULE, DELAYED REL PELLETS; ORAL
Prescription
No
AB
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