DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
PARLODEL
FDA Application No:
(NDA) 017962
Active Ingredient(s):
BROMOCRIPTINE MESYLATE
Company:
NOVARTIS
Original Approval or Tentative Approval Date:
June 28, 1978
Chemical Type:
1 New molecular entity (NME)
Review Classification:
P Priority 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
PARLODEL
BROMOCRIPTINE MESYLATE
EQ 2.5MG BASE
TABLET; ORAL
Prescription
Yes
AB
PARLODEL
BROMOCRIPTINE MESYLATE
EQ 5MG BASE
CAPSULE; ORAL
Prescription
Yes
AB
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