Cyclobenzaprine Hydrochloride Tablet, Film Coated
Product Images NDC 10702-006

10 FDA label images from Kvk-tech, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Cyclobenzaprine Hydrochloride (NDC 10702-006). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Kvk-tech, 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.

Product Images & Figures Index

FDA Label Image

Chemical Structure (Figure 01 Chemical Structure)

Chemical Structure (Figure 01 Chemical Structure)
Chemical structure of Cyclobenzaprine Hydrochloride showing the three-ring central structure bonded to an amine group and hydrochloride component, consistent with the generic drug Cyclobenzaprine Hydrochloride.*
FDA Label Image
Logo (Figure 02 Kvk Logo)
FDA Label Image

5mg-100s (Figure 03 5mg 100 Label)

5mg-100s (Figure 03 5mg 100 Label)
Label for Cyclobenzaprine Hydrochloride 5 mg film-coated tablets by KVK-TECH, Inc. The label indicates the product contains 5 mg of Cyclobenzaprine Hydrochloride per tablet, with 100 tablets per container. Usage directions, storage instructions, and a warning to keep out of children's reach are included. The NDC shown is 10702-006-01.*
FDA Label Image

5mg-500s (Figure 04 5mg 500 Label)

5mg-500s (Figure 04 5mg 500 Label)
Cyclobenzaprine Hydrochloride Tablets USP, 5 mg, film-coated oral tablets. The label indicates a package of 500 tablets. The labeler is KVK-TECH, Inc., located in Newtown, PA. The label includes dosage instructions for adults and storage conditions, along with a barcode and prescription only designation.*
FDA Label Image

5mg-1000s (Figure 05 5mg 1000 Label)

5mg-1000s (Figure 05 5mg 1000 Label)
Cyclobenzaprine Hydrochloride Tablets, USP 5 mg film-coated oral tablets in a package label showing 1000 tablets. The label displays dosage information, storage instructions, and warnings. The product is labeled for prescription use only and manufactured by KVK-TECH, Inc.*
FDA Label Image

10 mg-30s (Figure 06 10mg 30 Label)

10 mg-30s (Figure 06 10mg 30 Label)
Cyclobenzaprine Hydrochloride Tablets, USP 10 mg film-coated tablets packaging label from KVK-TECH, Inc. The label states each tablet contains 10 mg of Cyclobenzaprine Hydrochloride and includes dosage, storage, and dispensing instructions. The package contains 30 tablets and is intended for prescription use only.*
FDA Label Image

Figure 07 10mg 90 Label

Figure 07 10mg 90 Label
Cyclobenzaprine Hydrochloride 10 mg tablets, film coated, oral dosage form. The label shows product name, strength, and quantity of 90 tablets. It includes dosage instructions, storage conditions, a child-resistant packaging warning, manufacturer details (KVK-TECH, Inc.), and a barcode. The label is for prescription use only.*
FDA Label Image

Figure 08 10mg 100 Label

Figure 08 10mg 100 Label
Label for Cyclobenzaprine Hydrochloride Tablets, USP 10 mg, film-coated oral tablets, supplied in a bottle of 100 tablets. The label includes active ingredient strength, dosage form, storage instructions, dispensing guidance, manufacturer KVK-TECH, Inc., and an NDC barcode. The label also indicates prescription use only.*
FDA Label Image

Figure 09 10mg 500 Label

Figure 09 10mg 500 Label
Cyclobenzaprine Hydrochloride Tablets, USP 10 mg film-coated tablet container label by KVK-TECH, Inc. The label indicates a 500 tablet count with storage instructions and a warning to keep out of reach of children. The product is for oral use and labeled Rx only.*
FDA Label Image

Figure 10 10mg 1000 Label

Figure 10 10mg 1000 Label
Cyclobenzaprine Hydrochloride Tablets, USP 10 mg film-coated tablets packaging label from KVK-TECH, Inc. The label indicates a package size of 1000 tablets, includes dosage information, storage instructions, and a bar code with NDC 10702-007-10.*

* 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.