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; bronchospasm prophylaxis; asthma; copd 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).

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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 Code	Labeler / Repackager
42291-0621	AvKare, Inc.

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