Dronabinol Capsule
Product Images NDC 67877-755

8 FDA label images from Ascend Laboratories, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Dronabinol (NDC 67877-755). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ascend Laboratories, Llc, 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

Dronabinol-str.jpg (Dronabinol Str)

Dronabinol-str.jpg (Dronabinol Str)
Chemical structure diagram of dronabinol showing its molecular formula C21H30O2 with a molecular weight of 314.47.*
FDA Label Image

Dronabinol-fig.jpg (Dronabinol Fig)

Dronabinol-fig.jpg (Dronabinol Fig)
A line graph depicting mean appetite change from baseline over 6 weeks, comparing Dronabinol 2.5 mg BID with placebo. The vertical axis shows appetite change in mm VAS, and the horizontal axis shows time in weeks. Dronabinol shows a greater increase in appetite over time, with statistically significant differences at weeks 4 and 6 indicated by asterisks.*
FDA Label Image

Dronabinol-25-60cap-cont (Dronabinol 25 60cap Cont)

Dronabinol-25-60cap-cont (Dronabinol 25 60cap Cont)
Label for Dronabinol Capsules, USP 2.5 mg oral capsules by Ascend Laboratories, LLC. The label includes storage instructions, a warning about bottle seal integrity, and indicates the package contains 60 capsules. Manufacturer details for Patheon Softgels Inc. are also present alongside a barcode and NDC 67877-753-60.*
FDA Label Image

Dronabinol-25-60cap-cart (Dronabinol 25 60cap Cart)

Dronabinol-25-60cap-cart (Dronabinol 25 60cap Cart)
Packaging label for Dronabinol Capsules USP 2.5 mg by Ascend Laboratories, LLC. The label shows a unit-of-use prepack containing 60 capsules. It includes storage instructions and manufacturer info, stating the product is Rx only and dispensed with a prescription. The label features the NDC 67877-753-60 and indicates the capsules are in a prescription prepack form.*
FDA Label Image

Dronabinol-5-60cap-cont (Dronabinol 5 60cap Cont)

Dronabinol-5-60cap-cont (Dronabinol 5 60cap Cont)
Label for Dronabinol Capsules, USP 5 mg, oral capsules by Ascend Laboratories, LLC. The label indicates a package containing 60 capsules with each capsule containing 5 mg of dronabinol. It includes storage instructions and distributor and manufacturer information, along with the NDC number 67877-754-60.*
FDA Label Image

Dronabinol-5-60cap-cart (Dronabinol 5 60cap Cart)

Dronabinol-5-60cap-cart (Dronabinol 5 60cap Cart)
Packaging label for Dronabinol Capsules, USP 5 mg by Ascend Laboratories, LLC. The label indicates it is an oral capsule product with 60 capsules per bottle, marked Rx only. Storage instructions and manufacturing information by Patheon Softgels Inc., High Point, NC, are included. The label features barcode and NDC 67877-754-60.*
FDA Label Image

Dronabinol-10-60cap-cont (Dronabinol 10 60cap Cont)

Dronabinol-10-60cap-cont (Dronabinol 10 60cap Cont)
Label for Dronabinol Capsules USP 10 mg oral capsules, distributed by Ascend Laboratories, LLC and manufactured by Patheon Softgels Inc. The package contains 60 capsules. Storage instructions note keeping the product in a cool environment or refrigerated and protecting from freezing. The label includes an NDC code 67877-755-60 and a barcode.*
FDA Label Image

Dronabinol-10-60cap-cart (Dronabinol 10 60cap Cart)

Dronabinol-10-60cap-cart (Dronabinol 10 60cap Cart)
Packaging label for Dronabinol Capsules, USP 10 mg, an oral prescription drug by Ascend Laboratories, LLC. The label indicates a supply of 60 capsules, with storage instructions and manufacturer and distributor information. The NDC number 67877-755-60 and the Rx only designation are also shown.*

* 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.