Prescription Drug Information: Fluoxetine Hydrochloride (Page 11 of 11)

Principal Display Panel

Blister of 30
(click image for full-size original)

fluoxetine hydrochloride capsule
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:67046-211(NDC:0093-4356)
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
fluoxetine hydrochloride (fluoxetine) fluoxetine hydrochloride 20 mg
Product Characteristics
Color blue (aqua blue opaque) Score no score
Shape CAPSULE Size 16mm
Flavor Imprint Code 4356;20;mg
# Item Code Package Description Multilevel Packaging
1 NDC:67046-211-30 30 CAPSULE (CAPSULE) in 1 BLISTER PACK None
2 NDC:67046-211-60 60 CAPSULE (CAPSULE) in 1 BLISTER PACK None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA075245 04/05/2010
Labeler — Contract Pharmacy Services-PA (945429777)

Revised: 04/2010 Contract Pharmacy Services-PA provides trustworthy package insert and label information about marketed prescription drugs as submitted by manufacturers to the U.S. Food and Drug Administration. Package information is not reviewed or updated separately by Every individual prescription drug label and package insert entry contains a unique identifier which can be used to secure further details directly from the U.S. National Institutes of Health and/or the FDA.

As a leading independent provider of trustworthy medication information, we source our database directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. provides the full prescription-only subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Terms of Use | Copyright © 2022. All Rights Reserved.