Paxilcr
Product Images NDC 54868-5365

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Paxilcr (NDC 54868-5365). 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.

FDA Label Image

Paroxetine Hydrochloride Chemical Structural Formula (3601779b D19f 4915 8306 8806ac7823db 01)

Chemical structure diagram depicting the molecular structure of paroxetine hydrochloride, the active ingredient in PAXILCR CR. The diagram shows a fluorophenyl group, a piperidine ring, and a methylenedioxyphenyl group connected in the molecule.*

FDA Label Image

25-mg, 30-tablet Bottle Label (4791)

Packaging label for PAXILCR CR 25MG tablets distributed by Physicians Total Care, Inc., Tulsa, OK. The label shows the NDC 54868-4791-0, lot number, expiration date, manufacturer Gilead Smith Kline in Research Triangle, NC, and a barcode. The package contains 30 tablets.*

FDA Label Image

12.5-mg, 30-tablet Bottle Label (5347)

Label for PAXIL CR 12.5MG tablets, showing a 30 tablet count. The label includes the NDC number 54868-5347-0 and indicates Physicians Total Care, Inc. as the distributor. The lot number is 0000, with an expiration date listed as 01/60, and the product was manufactured by GLOCOM SMITH KLINE in Research Triangle, NC.*

FDA Label Image

37.5 mg, 30-tablet Bottle Label (5365)

The packaging label shows PAXIL CR 37.5MG, with 30 tablets distributed by Physicians Total Care, Inc., Tulsa, OK. It includes an NDC number (54868-5365-0), a lot number, expiration date (01/60), manufacturer information (GlaxoSmithKline Research Triangle NC 27709), and a barcode.*

* 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.