Paroxetine Tablet, Film Coated
Product Images NDC 68084-047

Product Visual Gallery

This gallery contains 16 technical images submitted to the FDA as part of the official labeling for Paroxetine (NDC 68084-047). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, 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

10 mg Blister

Label sheet containing multiple identical labels for Paroxetine tablets, USP 10 mg, film-coated, oral dosage form. Each label displays the product name, strength (10 mg), lot number (123456), expiration date (10/18), and is manufactured or labeled by American Health Packaging, Columbia, South Carolina.*

FDA Label Image

10 mg Carton

Paroxetine Tablets, USP 10 mg film-coated tablets packaging label. The label states the quantity of 100 tablets (10 x 10) and features a green accent box with the strength. It includes storage instructions, a pharmacist dispensing note, and distributor information from American Health Packaging, Columbus, Ohio.*

FDA Label Image

20 mg Blister

Label sheet for Paroxetine 20 mg oral film-coated tablets from American Health Packaging. Each label includes the drug name, strength, dosage form, barcode, lot number and expiration placeholders, and the manufacturer location in Columbus, Ohio. Multiple identical labels are shown on the sheet.*

FDA Label Image

20 mg Carton

Paroxetine Tablets, USP 20 mg film-coated oral tablets label from American Health Packaging. The label shows a package containing 100 tablets (10 blister packs of 10). It includes an NDC number 68084-045-01 and dispensing instructions for pharmacists. The label emphasizes prescription-only status and storage conditions.*

FDA Label Image

30 mg Blister

Labels for Paroxetine 30 mg tablet, USP, film-coated, oral dosage form. Each label displays the drug name, strength, lot number 123456, expiry date 08/18, and manufacturer American Health Packaging based in Columbia, OH. Several identical labels are shown in a sheet format with barcodes and identification numbers.*

FDA Label Image

30 mg Carton

Paroxetine 30 mg film-coated tablets label for oral use, displaying the drug name, strength, quantity of 100 tablets (10 x 10), and barcode. Label includes storage instructions, pharmacist dispensing guidance, drug protection warnings, and manufacturer details for American Health Packaging, Columbus, Ohio.*

FDA Label Image

40 mg Blister

The image shows multiple identical white labels for Paroxetine Tablets, USP 40 mg, film-coated oral tablets. Each label includes the drug name, strength, a barcode, placeholder text for lot number and expiry date, and the labeler, American Health Packaging, Columbus, Ohio.*

FDA Label Image

40 mg Carton

Paroxetine Tablets, USP 40 mg film-coated tablets in a package of 100 tablets (10 x 10). Label shows the product name, strength, NDC number 68084-047-01, manufacturer American Health Packaging, and usage instructions including storage conditions and a note for pharmacists to dispense a Medication Guide. The label also includes barcodes and cautions to keep drugs out of reach of children and not to use if blister is damaged.*

FDA Label Image

Ahp04401

Paroxetine 20 mg film-coated tablet shown with front and back views. The round white tablet has an imprint of "2C" above a scoreline and "15" below the scoreline. The image includes a millimeter scale for size reference. Labeled by American Health Packaging.*

FDA Label Image

Ahp04501

Paroxetine 20 mg film-coated tablets, round and white. One side is embossed with "ZC 16" while the other side is smooth and unmarked. The tablets are intended for oral administration and are supplied by American Health Packaging.*

FDA Label Image

Ahp04601

Paroxetine 10 mg film-coated round tablet, white, showing one side imprinted with "ZC17" and the other side plain. A size scale is included in the image. This product is labeled by American Health Packaging for oral use.*

FDA Label Image

Ahp04701

Paroxetine 30 mg film-coated tablet, oral use, displayed with front side imprinted with 'ZC18' and plain back side. The round, white tablet is shown against a gray background with millimeter scale for size reference. Labeler: American Health Packaging.*

FDA Label Image

Figure 1

A forest plot chart showing the fold change and 90% confidence interval of pharmacokinetic parameters (Cmax and AUC) for various interacting drugs (Pimozide 2 mg, Desipramine 100 mg, Propranolol 80 mg twice daily, Digoxin 0.25 mg once daily, Phenytoin 300 mg) relative to reference values. The x-axis represents change relative to reference on a logarithmic scale from 0.1 to 10.*

FDA Label Image

Figure 2

A horizontal scatter plot showing the fold change and 90% confidence intervals for Cmax and AUC pharmacokinetic parameters of Paroxetine when coadministered with interacting drugs including Cimetidine 300 mg three times daily, Phenobarbital 100 mg once daily, Phenytoin 300 mg once daily, Digoxin 0.25 mg once daily, and Diazepam 5 mg three times daily. The x-axis represents change relative to reference, ranging from 0 to 2.*

FDA Label Image

Figure 3

A forest plot chart depicting fold change and 90% confidence intervals for pharmacokinetic parameters (Cmax, AUC, Cmin) of Paroxetine across different population groups, including mild, moderate, and severe renal impairment, hepatic impairment, elderly age with various dosages, and males. The x-axis represents change relative to reference on a logarithmic scale ranging from 0.5 to 50.*

FDA Label Image

Structure

Chemical structure diagram of Paroxetine hydrochloride showing its fluorophenyl group and morpholine ring with detailed bonding.*

* 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.