DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
BRONKOSOL
FDA Application No:
(NDA) 012339
Active Ingredient(s):
ISOETHARINE HYDROCHLORIDE
Company:
SANOFI AVENTIS US
Chemical Type:
1 New molecular entity (NME)
Review Classification:
S Standard review drug
Therapeutic Equivalents
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Approval History and Related Documents are not available
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
BRONKOMETER
ISOETHARINE MESYLATE
0.34MG/INH
AEROSOL, METERED; INHALATION
Discontinued
No
None
BRONKOSOL
ISOETHARINE HYDROCHLORIDE
1%
SOLUTION; INHALATION
Discontinued
No
None
BRONKOSOL
ISOETHARINE HYDROCHLORIDE
0.25%
SOLUTION; INHALATION
Discontinued
No
None
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