DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
SALUTENSIN
FDA Application No:
(NDA) 012359
Active Ingredient(s):
HYDROFLUMETHIAZIDE; RESERPINE
Company:
SHIRE
Original Approval or Tentative Approval Date:
June 20, 1960
Chemical Type:
4 New combination
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
SALUTENSIN
HYDROFLUMETHIAZIDE; RESERPINE
50MG; 0.125MG
TABLET; ORAL
Discontinued
No
None
SALUTENSIN-DEMI
HYDROFLUMETHIAZIDE; RESERPINE
25MG; 0.125MG
TABLET; ORAL
Discontinued
No
None
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