Doxycycline Hyclate
Product Images NDC 67296-0329

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Doxycycline Hyclate (NDC 67296-0329). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

Epm Labels (67296 0329)

Labels for Doxycycline Hyclate 100 mg tablets in three package sizes: 14 tablets, 20 tablets, and 2 tablets. Each label includes NDC numbers (67296-0329-2, 67296-0329-3, 67296-0329-4), Rx Only designation, storage instructions (20-25 C), manufacturer information (Mutual Pharmaceutical Co., Inc. or Alkaloida Chemical Company Zrt.), distributor Redpharm Drug, Eden Prairie, MN, and barcodes for each package size.*

FDA Label Image

R:\regulatory\spl\jennifer\doxycycline Caps\pictures\doxycycline-01.jpg (Doxycycline 01)

Chemical structure diagram of Doxycycline Hyclate showing its molecular framework, including hydroxyl, methyl, amino, and other functional groups, along with associated HCl, ethanol (CH3CH2OH), and water (H2O) components.*

FDA Label Image

50 mg (Doxycycline 02)

Doxycycline Hyclate Capsules USP 50 mg label, equivalent to 50 mg doxycycline, from Sun Pharma. The label indicates a prescription product containing 50 capsules, includes storage instructions, warnings, and a barcode. Distributed by Sun Pharmaceutical Industries, Inc.*

FDA Label Image

50mg Alkaloida (Doxycycline 03)

Label for Doxycycline Hyclate Capsules USP 50 mg, containing 50 capsules per package. The label states the active ingredient as doxycycline hyclate equivalent to 50 mg doxycycline, with storage instructions and dosing caution. Manufactured by Alkaloida Chemical Company Zrt. in Hungary and distributed by Sun Pharmaceutical Industries, Inc. in Cranbury, NJ. The capsule is imprinted with 'MUTUAL 100'.*

FDA Label Image

R:\regulatory\spl\jennifer\doxycycline Caps\pictures\doxycycline-04.jpg (Doxycycline 04)

Doxycycline Hyclate Capsules USP 100 mg label showing strength and dosage form as capsules. The label states the product is Rx Only and contains 50 capsules. It includes storage instructions, dispensing warnings, and manufacturer information for Sun Pharmaceutical Industries, Inc. The label also displays a barcode and NDC number 53489-119-02.*

FDA Label Image

R:\regulatory\spl\jennifer\doxycycline Caps\pictures\doxycycline-05.jpg (Doxycycline 05)

Label for Doxycycline Hyclate Capsules USP 100 mg by Sun Pharma, containing 50 capsules. The label includes dosage equivalence, storage instructions to keep in a tight, light-resistant container at 20° to 25°C, and manufacturer information listing Alkaloida Chemical Company Zrt. in Hungary. The capsules are imprinted with 'MUTUAL 105'.*

FDA Label Image

R:\regulatory\spl\jennifer\doxycycline Caps\pictures\doxycycline-06.jpg (Doxycycline 06)

Label for Doxycycline Hyclate Tablets USP, 100 mg strength. The label states each tablet is equivalent to 100 mg doxycycline. It is an Rx only product containing 50 tablets in the package. The label includes storage instructions, warnings about light sensitivity, and disposal directions. The label identifies Sun Pharma as the manufacturer and includes an NDC code and barcode.*

FDA Label Image

R:\regulatory\spl\jennifer\doxycycline Caps\pictures\doxycycline-07.jpg (Doxycycline 07)

Label for Doxycycline Hyclate Tablets USP 100 mg, containing 50 tablets. The label provides dosage strength equivalent to 100 mg doxycycline, storage instructions, and manufacturer information including ALKALOID Chemical Company Zrt. in Hungary. Distributed by Sun Pharmaceutical Industries, Inc. The label includes a barcode and prescription-only designation.*

* 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.