Calcitriol Capsule
Product Images NDC 60687-345

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Calcitriol (NDC 60687-345). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, 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

Card Print Calcitriol 0.25 Mcg (0.25 Mcg Calcitriol Capsule Blister 01)

Label sheet for Calcitriol Capsules 0.25 mcg by American Health Packaging. Each label displays the product name and strength, along with a barcode, NDC number 60687-345-11, and placeholders for expiration date and lot number. The label indicates the oral capsule dosage form and the manufacturer location in Columbus, Ohio.*

FDA Label Image

Carton Label 0.25 mg (0.25 Mcg Calcitriol Caspules Carton)

Label for Calcitriol Capsules 0.25 mcg, containing 100 capsules (10 x 10) from American Health Packaging. The label shows the product name, strength, dosage form, count, NDC 60687-345-01, and includes storage instructions, usual dosage reference, and safety warnings. The label also identifies the distributor as American Health Packaging, Columbus, Ohio.*

FDA Label Image

Calcitriol (8f038f36 C63b 4484 B3e6 80a22401cc2f 01)

Chemical structure of calcitriol, the active ingredient in Calcitriol Capsules 0.25 mcg. The diagram depicts the molecule's steroid backbone with hydroxyl groups at positions 1, 3, and 25 as part of its chemical composition.*

FDA Label Image

B1797bb7 2098 B983 E053 2a95a90a68de

Calcitriol Capsules 0.25 mcg in oval, orange softgel form, one side marked with the imprint '673'. The image shows both the imprinted and opposite sides of the capsule. Labeler is American Health Packaging.*

* 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.