Pill Identifier Naltrexone Hydrochloride - NDC 47335-326
Naltrexone Hydrochloride
Product Code 47335-326
Naltrexone Hydrochloride by Sun Pharmaceutical Industries, Inc. is a yellow rou tablet film coated about 10 mm in size, imprinted with 326. The product is a human prescription drug with active ingredient(s) naltrexone hydrochloride.
Naltrexone Hydrochloride
Active Ingredient(s): Naltrexone Hydrochloride
Inactive Ingredient(s):
- LACTOSE MONOHYDRATE
- CELLULOSE, MICROCRYSTALLINE
- SILICON DIOXIDE
- CROSPOVIDONE
- MAGNESIUM STEARATE
- HYPROMELLOSE 2910 (6 MPA.S)
- TITANIUM DIOXIDE
- POLYETHYLENE GLYCOL 400
- FERRIC OXIDE YELLOW
- POLYSORBATE 80
- FERRIC OXIDE RED
Sun Pharmaceutical Industries, Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated
- Yellow (C48330)
Product Packages
| NDC Package Code | Package Description |
|---|---|
| 47335-326-08 | 100 TABLET, FILM COATED in 1 BOTTLE |
| 47335-326-18 | 1000 TABLET, FILM COATED in 1 BOTTLE |
| 47335-326-83 | 30 TABLET, FILM COATED in 1 BOTTLE |
| 47335-326-88 | 100 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.