Fetzima Capsule, Extended Release
Product Images NDC 0456-2280

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Fetzima (NDC 0456-2280). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Allergan, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Fetzima 01

Fetzima 01
Chemical structure diagram of levomilnacipran hydrochloride, the active ingredient in Fetzima oral medication. The structure shows molecular bonds and key functional groups typical to this compound.*
FDA Label Image

Fetzima 02

Fetzima 02
A chart depicting fold change and 90% confidence intervals for levomilnacipran hydrochloride (LVM) drug interactions involving CYP3A4 inhibitors, inducers, and substrates. The chart shows Cmax and AUC changes relative to reference when LVM is combined with ketoconazole, carbamazepine, and alprazolam, illustrating the impact on pharmacokinetics.*
FDA Label Image

Fetzima 03

Fetzima 03
A fold change and 90% confidence interval forest plot depicting pharmacokinetic parameters (Cmax and AUC) for different population subgroups: age above 65 years, gender (females), and various degrees of renal and hepatic impairment (mild, moderate, severe). The x-axis indicates change relative to reference values, illustrating variations in drug exposure across these populations.*
FDA Label Image

Fetzima 04

Fetzima 04
A Kaplan-Meier survival curve chart showing the proportion of patients with relapse over time (days) comparing Fetzima and placebo groups. The graph plots relapse rates from randomization to approximately 200 days, with Fetzima showing a lower relapse proportion than placebo. Patient counts at risk are listed below the x-axis across several time points.*
FDA Label Image

Fetzima 05

Fetzima 05
The packaging label for Fetzima levomilnacipran extended-release capsules, 20 mg per capsule. The label shows a carton panel with a 30-capsule count and includes usage instructions, storage conditions, and manufacturer details. It is distributed by Allergan USA, Inc., Madison, NJ.*
FDA Label Image

Fetzima 06

Fetzima 06
Label for Fetzima levomilnacipran extended-release capsules, 40 mg per capsule. The label states it is a prescription capsule product containing 30 capsules, distributed by Allergan USA, Inc. It includes storage instructions, dosage form, and notes that it is licensed from Pierre Fabre Medicament and made in France.*
FDA Label Image

Fetzima 07

Fetzima 07
Fetzima 80 mg extended-release capsules packaging label shows the proprietary name Fetzima and the generic name levomilnacipran. The label states it is for oral use, prescription only, and contains 30 capsules. It includes storage instructions, dosage form, and distributor Allergan USA, Inc. information.*
FDA Label Image

Fetzima 08

Fetzima 08
Fetzima 120 mg extended-release capsules label displaying the proprietary and generic name levomilnacipran hydrochloride, dosage strength, and dosage form. The label shows it is a prescription drug distributed by Allergan, Inc. It contains 30 capsules and includes storage instructions and safety warnings on the right side.*
FDA Label Image

Fetzima 09

Fetzima 09
Label for Fetzima levomilnacipran extended-release capsules Titration Pack by Allergan, Inc. The kit contains two 20 mg capsules and twenty-six 40 mg capsules. Directions include taking two 20 mg capsules once daily on Days 1 and 2, then one 40 mg capsule once daily from Day 3 through Day 28. The label features instructions for use and medication guide information.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.