DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
ZOCOR
FDA Application No:
(NDA) 019766
Active Ingredient(s):
SIMVASTATIN
Company:
MERCK
Original Approval or Tentative Approval Date:
December 23, 1991
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
ZOCOR
SIMVASTATIN
5MG
TABLET; ORAL
Prescription
No
AB
ZOCOR
SIMVASTATIN
10MG
TABLET; ORAL
Prescription
No
AB
ZOCOR
SIMVASTATIN
20MG
TABLET; ORAL
Prescription
No
AB
ZOCOR
SIMVASTATIN
40MG
TABLET; ORAL
Prescription
No
AB
ZOCOR
SIMVASTATIN
80MG
TABLET; ORAL
Prescription
Yes
AB
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