Skip to the page

Data / Drug companies / Selder, S.A. de C.V.

Selder, S.A. de C.V.: 8 products in the FDA NDC directory, labeler code 63654

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

Selder, S.A. de C.V. (labeler code 63654) lists 8 products in the FDA National Drug Code Directory, covering 5 finished drugs by generic name. By type: 8 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on April 10, 2024.

The request: Watch Selder, S.A. de C.V. (FDA labeler code 63654): each new product listing and each discontinued product. $10 of work on sign-up, no card.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Labeler code
63654
Products in commercial distribution
8
Packages
12
Finished drugs by generic name
5
Prescription products
0
Over the counter products
8
Flagged as original packager
8 of 8 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
November 15, 2011
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 drugs562.5%
Generic drugs (ANDA)337.5%

Products by type

TypeProductsShare
Over the counter drugs8100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Tablet675%
Capsule, liquid filled112.5%
Spray, metered112.5%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
XL - 3 Allergy63654-415TabletGeneric drugs (ANDA)April 10, 2024
Cold Medicine XL363654-605TabletOver the counter monograph drugsJune 27, 2022
Mucus Relief Xpect63654-342TabletOver the counter monograph drugsMay 17, 2021
Cold Medicine XL3 FORTE63654-601TabletOver the counter monograph drugsAugust 1, 2017
Fluticasone Propionate63654-380Spray, meteredGeneric drugs (ANDA)May 17, 2017
Allergy63654-309TabletGeneric drugs (ANDA)December 16, 2014
Cough and Cold XL3 Xtra63654-800Capsule, liquid filledOver the counter monograph drugsNovember 15, 2011
Cold Medicine63654-275TabletOver the counter monograph drugsNovember 15, 2011

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.