DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
AQUAMEPHYTON
FDA Application No:
(NDA) 012223
Active Ingredient(s):
PHYTONADIONE
Company:
ATON
Original Approval or Tentative Approval Date:
June 28, 1960
Chemical Type:
5 New manufacturer
Review Classification:
S Standard review drug
Therapeutic Equivalents
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Approval History, Letters, Reviews and Related Documents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
AQUAMEPHYTON
PHYTONADIONE
10MG/ML
INJECTABLE; INJECTION
Discontinued
No
None
AQUAMEPHYTON
PHYTONADIONE
1MG/0.5ML
INJECTABLE; INJECTION
Discontinued
No
None
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