Cymbalta
Product Images NDC 54868-5215

8 FDA label images from Physicians Total Care, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Cymbalta (NDC 54868-5215). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Physicians Total Care, 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.

Product Images & Figures Index

FDA Label Image

Image Of 20 mg Package Label (20mg Package Label)

Image Of 20 mg Package Label (20mg Package Label)
Physicians Total Care Cymbalta 20 mg capsule bottle label. Contains 90 capsules of duloxetine hydrochloride. Label includes federal cautions, usage instructions, storage conditions, and barcode with lot and expiration details.*
FDA Label Image

Image Of 30 mg Package Label (30mg Package Label)

Image Of 30 mg Package Label (30mg Package Label)
Cymbalta 30 mg capsules packaging label by Physicians Total Care, Inc. The label shows the product name, active ingredient duloxetine HCL, strength of 30 mg, and quantity of 60 capsules. It includes federal caution about prescription dispensing and storage instructions on the side panel.*
FDA Label Image

Image Of 60 mg Package Label (60mg Package Label)

Image Of 60 mg Package Label (60mg Package Label)
Package label for Cymbalta 60 mg capsules by Physicians Total Care, Inc. The label includes the active ingredient duloxetine HCl, a note stating federal law prohibits dispensing without prescription, and storage instructions to keep the medication in the original container, away from heat and moisture. The package contains 60 capsules and includes lot and expiration information.*
FDA Label Image

Image Of Chemical Structure (Chemical Structure)

Image Of Chemical Structure (Chemical Structure)
Chemical structure of Cymbalta (duloxetine), showing its molecular framework including aromatic rings, sulfur, oxygen atoms, and nitrogen with hydrochloride and methyl group components.*
FDA Label Image

Image Of Figure 1 (Figure 1)

Image Of Figure 1 (Figure 1)
A line graph showing the percentage of patients improved on the y-axis versus percent improvement in pain from baseline on the x-axis. The graph compares four groups labeled CYM 60mg BID, CYM 60mg QD, CYM 20mg QD, and Placebo, illustrating pain improvement outcomes in patients over a range of pain improvement percentages.*
FDA Label Image

Image Of Figure 2 (Figure 2)

Image Of Figure 2 (Figure 2)
A line graph showing the percentage of patients improved versus percent improvement in pain from baseline. The graph compares three groups: CYM 60mg BID, CYM 60mg QD, and placebo. The horizontal axis represents percent improvement in pain, while the vertical axis shows the percentage of patients improved, ranging from 0% to 100%.*
FDA Label Image

Image Of Figure 3 (Figure 3)

Image Of Figure 3 (Figure 3)
A line graph showing percentage of patients improved versus percent improvement in pain from baseline for Cymbalta 60mg twice daily, Cymbalta 60mg once daily, and placebo. The graph compares the effectiveness of Cymbalta dosages against placebo over ranges of pain improvement percentages.*
FDA Label Image

Image Of Figure 4 (Figure 4)

Image Of Figure 4 (Figure 4)
A line graph showing the percentage of patients improved versus percent improvement in pain from baseline. It compares Cymbalta (CYN) doses of 20 mg, 60 mg, and 120 mg once daily with a placebo, illustrating the relationship between dosage and patient improvement in pain reduction.*

* 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.