Pill Identifier Lansoprazole - NDC 62175-430
Lansoprazole
Product Code 62175-430
Lansoprazole by Lannett Company, Inc. is a pink capsule capsule delayed release pellets about 19 mm in size, imprinted with ku;430. The product is a human prescription drug with active ingredient(s) lansoprazole.
Lansoprazole
Active Ingredient(s): Lansoprazole
Inactive Ingredient(s):
- FD&C BLUE NO. 1
- FD&C RED NO. 3
- GELATIN
- HYPROMELLOSE 2910 (6 MPA.S)
- MAGNESIUM CARBONATE
- MANNITOL
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A
- POLYETHYLENE GLYCOL 6000
- POLYSORBATE 80
- SODIUM LAURYL SULFATE
- SODIUM STARCH GLYCOLATE TYPE A CORN
- SUGARCANE
- TALC
- TITANIUM DIOXIDE
- SHELLAC
- ISOPROPYL ALCOHOL
- BUTYL ALCOHOL
- AMMONIA
- ALCOHOL
- FERROSOFERRIC OXIDE
- ALUMINUM CHLOROHYDREX PROPYLENE GLYCOL
Lannett Company, Inc.
Product Type: Human Prescription Drug
Dosage Form: Capsule, Delayed Release Pellets
- Pink (C48328)
Product Packages
NDC Package Code | Package Description |
---|---|
62175-430-32 | 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE |
62175-430-37 | 100 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE |
62175-430-41 | 500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE |
62175-430-43 | 1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE |
62175-430-46 | 90 CAPSULE, DELAYED RELEASE PELLETS 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.