DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
LOPERAMIDE HYDROCHLORIDE
FDA Application No:
(NDA) 021855
Active Ingredient(s):
LOPERAMIDE HYDROCHLORIDE
Company:
BANNER PHARMACAPS
Original Approval or Tentative Approval Date:
August 4, 2005
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
LOPERAMIDE HYDROCHLORIDE
LOPERAMIDE HYDROCHLORIDE
1MG
CAPSULE; ORAL
OTC
No
None
LOPERAMIDE HYDROCHLORIDE
LOPERAMIDE HYDROCHLORIDE
2MG
CAPSULE; ORAL
OTC
Yes
None
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