Cyclobenzaprine Hydrochloride Tablet, Film Coated
Product Images NDC 72888-012

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Cyclobenzaprine Hydrochloride (NDC 72888-012). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advagen Pharma Limited, 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

Cyclobenzaprine HCl Tabs Structure

Chemical structure of cyclobenzaprine hydrochloride, showing the molecular arrangement and hydrochloride salt component represented by HCl in the formula.*

FDA Label Image

Ndc 72888-014-00 Bottles Of 1000 Tablets (Cyclobenzaprine HCl Tabs Usp 10mg 1000s)

Label for Cyclobenzaprine Hydrochloride Tablets, USP 10 mg, film-coated oral tablets. The label indicates the package contains 1000 tablets. It is distributed by Advagen Pharma Limited, Plainsboro, NJ, and manufactured by Rubicon Research Private Limited, Ambernath, India. The label includes storage instructions, caution to keep out of reach of children, and a child-resistant container notice.*

FDA Label Image

Ndc 72888-014-01 Bottles Of 100 Tablets (Cyclobenzaprine HCl Tabs Usp 10mg 100s)

Packaging label for Cyclobenzaprine Hydrochloride Tablets USP 10 mg, film-coated tablets. The label includes dosage details, storage instructions, NDC 72888-014-01, distributor Advagen Pharma Limited, and manufacturer Rubicon Research Private Limited. The package contains 100 tablets and features a barcode and an overprinting area.*

FDA Label Image

Ndc 72888-014-05 Bottles Of 500 Tablets (Cyclobenzaprine HCl Tabs Usp 10mg 500s)

Label for Cyclobenzaprine Hydrochloride tablets USP 10 mg, film-coated oral tablets. The package contains 500 tablets. Distributed by Advagen Pharma Limited and manufactured by Rubicon Research Private Limited in India. The label includes storage instructions, dosage caution, barcodes, and a designated overprinting area.*

FDA Label Image

Cyclobenzaprine HCl Tabs Usp 5mg 1000s

Label for Cyclobenzaprine Hydrochloride Tablets, USP 5 mg, film-coated oral tablets. The label states the product contains 5 mg cyclobenzaprine hydrochloride per tablet, with a package size of 1000 tablets. Distributed by Advagen Pharma Limited and manufactured by Rubicon Research Private Limited, India. Includes storage instructions and safety warnings.*

FDA Label Image

Ndc 72888-012-01 Bottles Of 100 Tablets (Cyclobenzaprine HCl Tabs Usp 5mg 100s)

Label for Cyclobenzaprine Hydrochloride Tablets, USP 5 mg by Advagen Pharma Limited. The film-coated tablet contains 5 mg cyclobenzaprine hydrochloride, available as a 100-count package. Label includes storage instructions (20-25°C), child-resistant container guidance, barcode, and distributor and manufacturer details with an overprinting area on the right side.*

FDA Label Image

Ndc 72888-012-05 Bottles Of 500 Tablets (Cyclobenzaprine HCl Tabs Usp 5mg 500s)

Label for Cyclobenzaprine Hydrochloride Tablets USP 5 mg, film-coated tablets in a 500-count package. Distributed by Advagen Pharma Limited and manufactured by Rubicon Research Private Limited. Storage instructions and safety warnings are included, along with barcodes and licensing information.*

FDA Label Image

Ndc 72888-013-01 Bottles Of 100 Tablets (Cyclobenzaprine HCl Tabs Usp 7 5mg 100s)

Label for Cyclobenzaprine Hydrochloride Tablets, USP 7.5 mg, film-coated oral tablets. The label states the active ingredient strength as 7.5 mg and the package contains 100 tablets. It is distributed by Advagen Pharma Limited and manufactured by Rubicon Research Private Limited. Includes storage instructions, NDC 72888-013-01, and a barcode. The label also features a designated overprinting area.*

* 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.