Pill Identifier Fluoxetine Hydrochloride - NDC 49884-335
Fluoxetine Hydrochloride
Product Code 49884-335
Fluoxetine Hydrochloride by Par Pharmaceutical, Inc. is a white oval tablet coated about 10 mm in size, imprinted with ep;360. The product is a human prescription drug with active ingredient(s) fluoxetine hydrochloride.
Fluoxetine Hydrochloride
Active Ingredient(s): Fluoxetine Hydrochloride
Inactive Ingredient(s):
- SILICON DIOXIDE
- STARCH, CORN
- CROSPOVIDONE
- MAGNESIUM STEARATE
- CELLULOSE, MICROCRYSTALLINE
- POLYVINYL ALCOHOL, UNSPECIFIED
- TITANIUM DIOXIDE
- TALC
- POLYETHYLENE GLYCOL, UNSPECIFIED
Par Pharmaceutical, Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Coated
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
49884-335-01 | 100 TABLET, COATED in 1 BOTTLE, PLASTIC |
49884-335-10 | 1000 TABLET, COATED in 1 BOTTLE, PLASTIC |
49884-335-11 | 30 TABLET, COATED in 1 BOTTLE, PLASTIC |
49884-335-82 | 2000 TABLET, COATED in 1 BOTTLE, PLASTIC |
* 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.