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Duloxetine Capsule, Delayed Release
Product Images NDC 52427-791
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Duloxetine (NDC 52427-791). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Almatica Pharma Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Figure1 (Figure 1)
A Kaplan-Meier curve graph showing the proportion of patients with relapse over time in days from randomization, comparing treatment with Duloxetine versus placebo. The graph depicts relapse rates over a span of 0 to 200 days, with Duloxetine showing a lower proportion of relapse compared to placebo.*
Figure2 (Figure 2)
A Kaplan-Meier survival curve chart comparing the proportion of patients with relapse over time (in days) from randomization between two treatments: Duloxetine and placebo. The graph shows relapse proportion on the vertical axis and time in days on the horizontal axis, with Duloxetine represented by a solid line and placebo by a dashed line.*
Label-120mg (Label 120mg)
Label for Duloxetine Delayed-Release Capsules 120 mg in a 30-capsule package by Almatica Pharma LLC. The label includes the NDC 52427-791-30, dosing information indicating 134.7 mg duloxetine hydrochloride equivalent to 120 mg duloxetine per capsule, storage instructions, and a pharmacist advisory to dispense the Medication Guide separately.*
Label-80mg (Label 80mg)
Label for Duloxetine Delayed-Release Capsules 80 mg by Almatica Pharma LLC. The label notes each capsule contains 89.8 mg duloxetine hydrochloride USP, equivalent to 80 mg duloxetine. Packaging indicates 30 capsules per container with storage instructions and prescription-only status.*
Label-90mg (Label 90mg)
Duloxetine Delayed-Release Capsules 90 mg label. The label indicates the product is for prescription use only, contains 30 capsules, and is distributed by Almatica Pharma LLC. The label displays storage instructions, dosage equivalence to duloxetine hydrochloride, and a barcode.*
Structure (Structure)
Chemical structure diagram of Duloxetine hydrochloride, showing the molecular arrangement including a thiophene ring, a naphthalene moiety, and associated functional groups.*
* 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.
