DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
PARAGARD T 380A
FDA Application No:
(NDA) 018680
Active Ingredient(s):
COPPER
Company:
DURAMED PHARMS BARR
Original Approval or Tentative Approval Date:
November 15, 1984
Chemical Type:
3 New dosage form
Review Classification:
S Standard review drug
There are no 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
PARAGARD T 380A
COPPER
309MG/COPPER
INTRAUTERINE DEVICE; INTRAUTERINE
Prescription
Yes
None
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