DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
LANOXICAPS
FDA Application No:
(NDA) 018118
Active Ingredient(s):
DIGOXIN
Company:
SMITHKLINE BEECHAM
Original Approval or Tentative Approval Date:
July 26, 1982
Chemical Type:
3 New dosage form
Review Classification:
S Standard review drug
There are no Therapeutic Equivalents
Labels are not available
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
LANOXICAPS
DIGOXIN
0.2MG
CAPSULE; ORAL
Prescription
Yes
None
LANOXICAPS
DIGOXIN
0.05MG
CAPSULE; ORAL
Prescription
No
None
LANOXICAPS
DIGOXIN
0.1MG
CAPSULE; ORAL
Prescription
No
None
LANOXICAPS
DIGOXIN
0.15MG
CAPSULE; ORAL
Discontinued
No
None
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