DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
PROTONIX
FDA Application No:
(NDA) 020987
Active Ingredient(s):
PANTOPRAZOLE SODIUM
Company:
WYETH PHARMS INC
Original Approval or Tentative Approval Date:
February 2, 2000
Chemical Type:
1 New molecular entity (NME)
Review Classification:
S Standard review drug
Therapeutic Equivalents
Label Information
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
PROTONIX
PANTOPRAZOLE SODIUM
EQ 40MG BASE
TABLET, DELAYED RELEASE; ORAL
Prescription
Yes
AB
PROTONIX
PANTOPRAZOLE SODIUM
EQ 20MG BASE
TABLET, DELAYED RELEASE; ORAL
Prescription
No
AB
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