Pill Identifier Montelukast Sodium - NDC 62175-210
Montelukast Sodium
Product Code 62175-210
Montelukast Sodium by Lannett Company, Inc. is a white rou tablet film coated about 8 mm in size, imprinted with ku;210. The product is a human prescription drug with active ingredient(s) montelukast sodium.
Montelukast Sodium
Active Ingredient(s): Montelukast Sodium
Inactive Ingredient(s):
- SILICON DIOXIDE
- CROSCARMELLOSE SODIUM
- HYDROXYPROPYL CELLULOSE (1600000 WAMW)
- MANNITOL
- CELLULOSE, MICROCRYSTALLINE
- POLYETHYLENE GLYCOL, UNSPECIFIED
- POLYVINYL ALCOHOL, UNSPECIFIED
- SODIUM STEARYL FUMARATE
- TALC
- TITANIUM DIOXIDE
Lannett Company, Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
62175-210-32 | 30 TABLET, FILM COATED in 1 BOTTLE |
62175-210-43 | 1000 TABLET, FILM COATED in 1 BOTTLE |
62175-210-46 | 90 TABLET, FILM COATED in 1 BOTTLE |
* Please review the disclaimer below.
Pill Identification data last updated on: December, 2018
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product. If this is an emergency, call 911 or the national Poison Help hotline at 1-800-222-1222. Most images are not part of the product labels and have not been verified by the labeler company. ALWAYS consult your physician or pharmacist with any medication-related questions.