Cipro Tablet, Film Coated
Product Images NDC 50419-758

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Cipro (NDC 50419-758). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bayer Healthcare Pharmaceuticals 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

Chem Struc 1 (Image 01)

Chemical structure diagram of ciprofloxacin hydrochloride monohydrate, showing its bicyclic quinolone core with a fluorine atom, piperazine ring, and associated hydrochloride and water components.*

FDA Label Image

Step 1 (Image 02)

An illustration showing two bottles of different sizes, both with ribbed caps. The bottles appear to be generic containers, likely representing medication bottles without visible labels or text.*

FDA Label Image

Step 2 (Image 03)

An instructional diagram showing how to open a child-resistant bottle cap by pressing down and turning. The illustration features two bottles with caps and an arrow indicating the opening direction and mechanism.*

FDA Label Image

Step 3 (Image 04)

An illustration showing how to pour or transfer liquid from one small bottle into another. The image depicts a tilted bottle pouring liquid into the open mouth of a second bottle below it.*

FDA Label Image

Step 4 (Image 05)

An illustration showing a film-coated tablet bottle with a child-resistant cap and a double-headed arrow beneath it, indicating the bottle's length or orientation.*

FDA Label Image

Chem Struc 2 (Image 06)

Chemical structure of ciprofloxacin hydrochloride, the active ingredient in Cipro tablets, as shown in the image.*

FDA Label Image

250 mg Label (Image 07)

Label for Cipro (ciprofloxacin hydrochloride) 250 mg film-coated tablets. The bottle contains 100 tablets and is labeled for prescription use only. Manufactured by Bayer HealthCare Pharmaceuticals Inc., Whippany, NJ, and produced in Germany. The label highlights pharmacist instructions to dispense the enclosed Medication Guide with the product.*

FDA Label Image

Cipro 500 mg (Image 08)

Cipro 500 mg ciprofloxacin hydrochloride film coated tablets label by Bayer HealthCare Pharmaceuticals Inc. The package contains 100 tablets and is for oral use. The label warns pharmacists to dispense the enclosed Medication Guide and includes storage instructions to keep below 86°F (30°C). Manufactured in Germany and printed in the USA.*

FDA Label Image

5 Carton (Image 09)

Cipro 5% Oral Suspension (ciprofloxacin oral suspension) bottle label for oral use only. Contains 5 g/100 mL with 250 mg ciprofloxacin per 5 mL. Manufactured by Bayer HealthCare Pharmaceuticals Inc. Includes instructions for preparation with microcapsules and suspension diluent along with pharmacist dispensing information and storage recommendations.*

FDA Label Image

10 Carton (Image 10)

Cipro 10% Oral Suspension label showing ciprofloxacin hydrochloride 10 g/100 mL (500 mg/5 mL) oral suspension. The label indicates it is for oral use only and must be reconstituted before dispensing. It includes directions about the components—microcapsules, suspension diluent, and a graduated 5 mL spoon—with manufacturer Bayer HealthCare Pharmaceuticals Inc. It also highlights storage instructions and precautions for administration.*

FDA Label Image

Gradated Spoon (Image 11)

An instructional diagram illustrating a measuring spoon with volume markings for 1/1 and 1/2. The image is likely intended to guide measurement or dosing but does not display any specific pharmaceutical product information.*

* 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.