DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
SSD AF
FDA Application No:
(NDA) 018578
Active Ingredient(s):
SILVER SULFADIAZINE
Company:
BASF
Original Approval or Tentative Approval Date:
February 25, 1982
Chemical Type:
5 New manufacturer
Review Classification:
S Standard review drug
There are no Therapeutic Equivalents
Labels are not available
Approval History, Letters, Reviews and Related Documents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
SSD
SILVER SULFADIAZINE
1%
CREAM; TOPICAL
Prescription
No
AB
SSD AF
SILVER SULFADIAZINE
1%
CREAM; TOPICAL
Prescription
No
BX
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