Pill Identifier Moexipril Hydrochloride - NDC 68462-208
Moexipril Hydrochloride
Product Code 68462-208
Moexipril Hydrochloride by Glenmark Pharmaceuticals Inc., Usa is a brow rou tablet film coated about 8 mm in size, imprinted with g;208. The product is a human prescription drug with active ingredient(s) moexipril hydrochloride.
Moexipril Hydrochloride
Active Ingredient(s): Moexipril Hydrochloride
Inactive Ingredient(s):
- CROSPOVIDONE (15 MPA.S AT 5%)
- LACTOSE MONOHYDRATE
- MAGNESIUM OXIDE
- MAGNESIUM STEARATE
- POVIDONE, UNSPECIFIED
- HYDROXYPROPYL CELLULOSE, UNSPECIFIED
- TITANIUM DIOXIDE
- POLYETHYLENE GLYCOL 6000
- FERRIC OXIDE RED
- FERROSOFERRIC OXIDE
- FERRIC OXIDE YELLOW
- HYPROMELLOSE, UNSPECIFIED
Glenmark Pharmaceuticals Inc., Usa
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated
- Brown (C48332)
Product Packages
NDC Package Code | Package Description |
---|---|
68462-208-01 | 100 TABLET, FILM COATED in 1 BOTTLE |
68462-208-10 | 1000 TABLET, FILM COATED in 1 BOTTLE |
68462-208-90 | 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.