Pill Identifier Fluoxetine Hydrochloride - NDC 51672-5306
Fluoxetine Hydrochloride
Product Code 51672-5306
Fluoxetine Hydrochloride by Taro Pharmaceuticals U.s.a., Inc. is a white capsule tablet film coated about 14 mm in size, imprinted with ac;398. The product is a human prescription drug with active ingredient(s) fluoxetine hydrochloride.
Fluoxetine Hydrochloride
Active Ingredient(s): Fluoxetine Hydrochloride
Inactive Ingredient(s):
- CELLULOSE, MICROCRYSTALLINE
- HYPROMELLOSE 2910 (3 MPA.S)
- HYPROMELLOSE 2910 (6 MPA.S)
- MAGNESIUM STEARATE
- MANNITOL
- POLYETHYLENE GLYCOL 400
- POLYSORBATE 80
- POVIDONE K30
- STARCH, CORN
- TITANIUM DIOXIDE
Taro Pharmaceuticals U.s.a., Inc.
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
51672-5306-2 | 500 TABLET, FILM COATED in 1 BOTTLE |
51672-5306-6 | 30 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.