Lomedia 24 Fe
Product Images NDC 65162-316

8 FDA label images from Amneal Pharmaceuticals Of New York, 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 Lomedia 24 Fe (NDC 65162-316). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Of New York, 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

Chem Struc 1 (Lomedia 24 Fe 1)

Chem Struc 1 (Lomedia 24 Fe 1)
Chemical structure of the active ingredient shown in the image, depicting a steroid-like molecular framework with hydroxyl, methyl, and ethynyl functional groups.*
FDA Label Image

Chem Struc 2 (Lomedia 24 Fe 2)

Chem Struc 2 (Lomedia 24 Fe 2)
Chemical structure diagram of the active ingredient associated with Lomedia 24 Fe, depicting carbon, hydrogen, and oxygen atoms arranged in a steroid-like molecular framework with specific functional groups including a ketone and an alkyne substituent.*
FDA Label Image

Figure 1 (Lomedia 24 Fe 3)

Figure 1 (Lomedia 24 Fe 3)
A line graph showing Norethindrone concentration (pg/mL) over time (hours). Two curves are displayed: one for Day 1 (solid circles) and another for Day 24 (open circles). Both curves show a rapid peak followed by a gradual decline, with the Day 24 curve generally higher than Day 1 across the timeline up to 60 hours.*
FDA Label Image

Figure 2 (Lomedia 24 Fe 4)

Figure 2 (Lomedia 24 Fe 4)
A line graph depicting Ethinyl Estradiol concentration (pg/mL) over time (hours) on Day 1 and Day 24. The graph shows two curves: a solid line for Day 1 and a dotted line for Day 24, each illustrating concentration changes from 0 to 60 hours.*
FDA Label Image

Figure 3 (Lomedia 24 Fe 5)

Figure 3 (Lomedia 24 Fe 5)
A bar chart depicting mortality rates per 100,000 woman users by age group (15-24, 25-34, 35-44, 45-) across four categories: Ever-Users (Nonsmokers), Ever-Users (Smokers), Controls (Nonsmokers), and Controls. The chart shows increasing mortality rates with age, with the highest rates observed in Ever-Users (Smokers) aged 45 and above.*
FDA Label Image

Inst Pack (Lomedia 24 Fe 6)

Inst Pack (Lomedia 24 Fe 6)
Lomedia 24 Fe oral contraceptive medication blister card from Amneal Pharmaceuticals of New York, LLC. The card is organized with 4 weeks of tablets arranged in horizontal rows starting from Sunday to Saturday, with arrows guiding the order of use. It contains 24 active therapy tablets and includes Norethindrone Acetate, Ethinyl Estradiol, and Ferrous Fumarate. The card includes a label with the proprietary name, NDC 65162-316-58, and instructions for daily use.*
FDA Label Image

Inst Pack (Lomedia 24 Fe 7)

Inst Pack (Lomedia 24 Fe 7)
Lomedia 24 Fe oral contraceptive tablet blister pack label by Amneal Pharmaceuticals of New York, LLC. The label shows a 4-week layout marking each day Sunday through Saturday with arrows indicating pill-taking direction. It highlights 24 days of active therapy with ingredients Norethindrone Acetate 1 mg, Ethinyl Estradiol 20 mcg, and Ferrous Fumarate 75 mg. The label includes NDC 65162-316 and instructions for starting on Sunday or Day 1 of the period.*
FDA Label Image

Carton (Lomedia 24 Fe 8)

Carton (Lomedia 24 Fe 8)
Packaging label for Lomedia 24 Fe tablets, containing norethindrone acetate 1 mg, ethinyl estradiol 20 mcg, and ferrous fumarate 75 mg. The carton states it provides 24 days of active therapy with a 28-day regimen. The product is manufactured by Watson Laboratories, Inc. and distributed by Amneal Pharmaceuticals of New York, LLC. The carton holds 3 dispensers, each containing one blister card of 28 tablets. Includes product warnings and use 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.