DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
PHENERGAN FORTIS
FDA Application No:
(NDA) 008381
Active Ingredient(s):
PROMETHAZINE HYDROCHLORIDE
Company:
ANI PHARMS
Original Approval or Tentative Approval Date:
April 11, 1952
Chemical Type:
2 New active ingredient
Review Classification:
S Standard review drug
Therapeutic Equivalents
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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
PHENERGAN FORTIS
PROMETHAZINE HYDROCHLORIDE
25MG/5ML
SYRUP; ORAL
Discontinued
No
None
PHENERGAN PLAIN
PROMETHAZINE HYDROCHLORIDE
6.25MG/5ML
SYRUP; ORAL
Discontinued
No
None
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