Pill Identifier Fluoxetine Hydrochloride - NDC 16714-114
Fluoxetine Hydrochloride
Product Code 16714-114
Fluoxetine Hydrochloride by Northstar Rx Llc is a white capsule tablet film coated about 14 mm in size, imprinted with f;60;2;63. The product is a human prescription drug with active ingredient(s) fluoxetine hydrochloride.
Fluoxetine Hydrochloride
Active Ingredient(s): Fluoxetine Hydrochloride
Inactive Ingredient(s):
- Croscarmellose Sodium
- Hypromelloses
- Polyethylene Glycol, Unspecified
- Povidone
- Starch, Pregelatinized Corn
- Microcrystalline Cellulose
- Magnesium Stearate
- Titanium Dioxide
Northstar Rx Llc
Product Type: Human Prescription Drug
Dosage Form: Tablet, Film Coated
- White (C48325)
Product Packages
NDC Package Code | Package Description |
---|---|
16714-114-01 | 30 TABLET, FILM COATED in 1 BOTTLE |
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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.