Tramadol Hydrochloride Tablet, Extended Release
Product Images NDC 47335-860

View Photos of 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 Tramadol Hydrochloride (NDC 47335-860). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Tramadol-figure1 (Tramadol Figure1)

Tramadol-figure1 (Tramadol Figure1)
Tramadol is a type of medication that comes in two forms: extended-release tablets with a dosage of 200mg taken once daily and immediate-release tablets with a dosage of 50mg taken every six hours. This text may be part of the informed consent document for taking Tramadol.*
FDA Label Image

Tramadol-figure2 (Tramadol Figure2)

Tramadol-figure2 (Tramadol Figure2)
This is a prescription medication information sheet for Tramadol Hydrochloride Extended-Release Tablets in 200 mg dose and Tramadol IR Tablets in 50 mg dose. The information does not provide any details on the purpose, usage, or side-effects of these medications.*
FDA Label Image

Tramadol-figure3 (Tramadol Figure3)

FDA Label Image

Tramadol-figure4 (Tramadol Figure4)

Tramadol-figure4 (Tramadol Figure4)
This text appears to be a caption for a figure showing a study on Tramadol Hydrochloride Extended-Release Tablets used for arthritis pain relief. The figure appears to show the percentage of patients achieving various levels of pain relief (measured on a VAS scale) over placebo. The text also indicates the use of response threshold (percent improvement from baseline) as a measure. No further information can be obtained from this output.*
FDA Label Image

Tramadol-label-100mg (Tramadol Label 100mg)

Tramadol-label-100mg (Tramadol Label 100mg)
This is a label of Tramadol Hydrochloride Extended-Release Tablets with dosage instructions. It is advised to swallow the tablets whole with liquid and not to split, chew, dissolve or crush them. The label also indicates that it is a prescription drug and the pharmacist should dispense it with medication. Additionally, it states that a guide is provided separately to each patient.*
FDA Label Image

Tramadol-label-200mg (Tramadol Label 200mg)

Tramadol-label-200mg (Tramadol Label 200mg)
Each tablet contains 200 mg of tramadol hydrochloride, USP, manufactured by Sun Pharmaceutical Industries Ltd. The usual dosage should be determined by the prescribing information. The tablets should be swallowed whole and stored in a tight, light-resistant container not accessible to children, at 20° to 25°C (68° to 77°F) with liquid, and not chewed, dissolved or crushed. Dispensing pharmacists must provide a medication guide separately. Distributed by Sun Pharmaceutical Industries, Inc. 30 tablets in each pack.*
FDA Label Image

Tramadol-label-300mg (Tramadol Label 300mg)

Tramadol-label-300mg (Tramadol Label 300mg)
This is a medication containing 300 mg of Tramadol Hydrochloride. It is an extended-release tablet that should be swallowed whole and not split, chewed, dissolved or crushed. Each tablet comes with prescribing information and should be dispensed with a medication guide. It is recommended to store the medication in a tight, light-resistant container at a temperature between 20 to 25 degrees Celsius. The medication is distributed by Sun Pharmaceutical Industries, Inc. in Cranbury, NJ. However, the manufacturer, Sun Pharmaceutical Industries Ltd, is located in Halol-Baroda Highway, Halol-389 350, Gujarat, India.*
FDA Label Image

Tramadol-structure (Tramadol Structure)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.