KU 210 (Montelukast sodium 10 mg (base))

This pill with imprint "KU 210" is White, Round and has been identified as Montelukast sodium 10 mg (base). It is manufactured by Kremers Urban Pharmaceuticals Inc..

Montelukast is used in the treatment of allergic rhinitis; asthma, maintenance; bronchospasm prophylaxis; copd; 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 Substance Act (CSA).

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

Manufacturer:

Kremers Urban Pharmaceuticals Inc.

National Drug Code (NDC):

62175-0210

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.

Imprint Code FAQ's

Other Manufacturers / Repackagers:

NDC Code	Manufacturer / Repackager
42291-0621	AvKare, Inc.

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