Paroxetine Hydrochloride Tablet, Film Coated, Extended Release
Product Images NDC 62175-472

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Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Paroxetine Hydrochloride (NDC 62175-472). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lannett Company, 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

Structural Formula (Paroxetine Extended Release Tablets Usp 1)

FDA Label Image

12.5 mg 30 Count Bottle Label (Paroxetine Extended Release Tablets Usp 2)

FDA Label Image

25 mg 30 Count Bottle Label (Paroxetine Extended Release Tablets Usp 3)

FDA Label Image

37.5 mg 30 Count Bottle Label (Paroxetine Extended Release Tablets Usp 4)

37.5 mg 30 Count Bottle Label (Paroxetine Extended Release Tablets Usp 4)
This appears to be a table of population descriptions for a medical study. It includes information on renal impairment, hepatic impairment, age, gender, PK (pharmacokinetics) measurements such as Cmax and AUC, and fold change with 90% confidence interval. Without further context it's difficult to determine the exact purpose of this table, but it may be useful for researchers or healthcare professionals evaluating a drug therapy.*
FDA Label Image

Paroxetine Extended Release Tablets Usp 5

Paroxetine Extended Release Tablets Usp 5
This is a medication description for Paroxetine Extended-Release Tablets, USP. The recommended usual dosage is not provided and needs to be checked on the accompanying prescribing information. It is important to use safe dosages when dispensing the product unless otherwise directed by the physician or requested by the purchase. Swallow the tablets whole and do not chew or crush them. The tablets are imported and specially designed for hydrochloride equivalent to 12.5 mg paroxetine. The manufacturer is Lomet Company located in Philadelphia, PA. The provided NDC code is 62175-470-32. The product comes in a package of 30 tablets, and it is essential to review the printed medication guide or check with Jomet company's website for more details.*
FDA Label Image

Paroxetine Extended Release Tablets Usp 6

Paroxetine Extended Release Tablets Usp 6
The text seems to be a description of medication called Paroxetine Extended-Release Tablets. It includes information about the safety measures that need to be taken while consuming the medicine. The usual dosage of the medication is mentioned as 5 grams. The medicine needs to be swallowed whole and not chewed or crushed. The text also provides details about the manufacturing company and a website to obtain more information.*
FDA Label Image

Paroxetine Extended Release Tablets Usp 7

Paroxetine Extended Release Tablets Usp 7
This is a medication guide for Paroxetine Extended-Release Tablets, USP. The guide includes information on the usual dosage, instructions for taking the tablets (swallow whole and do not chew or crush), and important warnings related to the usage of the medication. The tablets are manufactured by Lannett Company and are only available through prescription by a physician or other qualified healthcare provider. The document includes a product code and a revision number (CAT6408E Rev. 10/20).*

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