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Data / Drug companies / Belmora LLC

Belmora LLC: 24 products in the FDA NDC directory, labeler code 27854

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Belmora LLC (labeler code 27854) lists 24 products in the FDA National Drug Code Directory, covering 14 finished drugs by generic name. By type: 24 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on May 27, 2025.

The request: Watch Belmora LLC (FDA labeler code 27854): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
27854
Products in commercial distribution
24
Packages
29
Finished drugs by generic name
14
Prescription products
0
Over the counter products
24
Flagged as original packager
21 of 21 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
January 23, 2017
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Over the counter monograph drugs1458.3%
Generic drugs (ANDA)1041.7%

Products by type

TypeProductsShare
Over the counter drugs24100%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

Dosage forms

Dosage formProductsShare
Tablet, film coated625%
Tablet312.5%
Gel28.3%
Patch28.3%
Suspension28.3%
Capsule, liquid filled14.2%
Solution14.2%
Lotion14.2%
Jelly14.2%
Liquid14.2%
Tablet, chewable14.2%
Liniment14.2%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Chest Rub27854-399JellyOver the counter monograph drugsMay 27, 2025
Ivermectin27854-334LotionGeneric drugs (ANDA)August 12, 2024
Flanax27854-499LinimentOver the counter monograph drugsAugust 1, 2024
Cafiaspirina Rapid Headache Relief27854-755PowderOver the counter monograph drugsJune 30, 2024
Sedalmex forte27854-303TabletOver the counter monograph drugsJune 1, 2024
Childrens FLANAX ORAL27854-777SuspensionGeneric drugs (ANDA)January 26, 2024
Melox27854-117LiquidOver the counter monograph drugsMay 1, 2023
AnaDent Childrens Kanka Gel27854-178GelOver the counter monograph drugsNovember 8, 2022
Anadent Kanka Gel27854-177GelOver the counter monograph drugsApril 15, 2022
Sedalmex XL Flu27854-350Tablet, film coatedOver the counter monograph drugsMarch 24, 2022
Complete Cold Relief27854-299SolutionOver the counter monograph drugsFebruary 23, 2022
Regular Strength Pain Relief27854-388Capsule, liquid filledOver the counter monograph drugsJanuary 5, 2022
Flanax Back Pain Relief27854-333PatchOver the counter monograph drugsDecember 15, 2021
Belmora Flanax27854-555TabletGeneric drugs (ANDA)July 20, 2020
Ana-Dent PAIN RELIEF27854-701Tablet, film coatedGeneric drugs (ANDA)May 15, 2020
Flanax Pain Reliever/Fever Reducer27854-700Tablet, film coatedGeneric drugs (ANDA)May 15, 2020
Flanax Pain Reliever/Fever reducer27854-505Tablet, coatedGeneric drugs (ANDA)May 15, 2020
Flanax back pain relief27854-311PatchOver the counter monograph drugsFebruary 1, 2020
Nocto Sleep Aid27854-375TabletGeneric drugs (ANDA)October 31, 2019
Belmora MELOX AGRURA27854-120Tablet, chewableOver the counter monograph drugsJune 3, 2019
Melox27854-115SuspensionOver the counter monograph drugsJune 1, 2018
Flanax27854-160Tablet, film coatedGeneric drugs (ANDA)January 15, 2018
AnaDent27854-170Tablet, film coatedGeneric drugs (ANDA)January 23, 2017
Flanax Menstrual Pain Reliever27854-165Tablet, film coatedGeneric drugs (ANDA)January 23, 2017

CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.