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KU 210 (Montelukast Sodium 10 mg (base))

Pill with imprint KU 210 is White, Round and has been identified as Montelukast Sodium 10 mg (base). It is supplied by Kremers Urban Pharmaceuticals Inc..

Montelukast is used in the treatment of allergic rhinitis; asthma, maintenance; copd; bronchospasm prophylaxis; asthma and belongs to the drug class leukotriene modifiers. There is no proven risk in humans during pregnancy. Montelukast 10 mg (base) is not a controlled substance under the Controlled Substances Act (CSA).

Images for KU 210

Montelukast Sodium

Imprint:
KU 210
Strength:
10 mg (base)
Color:
White
Shape:
Round
Availability:
Prescription only
Drug Class:
Leukotriene modifiers
Pregnancy Category:
B - No proven risk in humans
CSA Schedule:
Not a controlled drug
Labeler / Supplier:
Kremers Urban Pharmaceuticals Inc.
Inactive Ingredients:
silicon dioxide
croscarmellose sodium
hydroxypropyl cellulose (type h)
mannitol
microcrystalline cellulose
polyethylene glycol
polyvinyl alcohol
sodium stearyl fumarate
magnesium silicate
titanium dioxide
Note: Inactive ingredients may vary.

Other Labelers / Repackagers:

NDC CodeLabeler / Repackager
42291-0621 AvKare, Inc.

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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