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Data / Drug companies / Cilag AG

Cilag AG: 7 products in the FDA NDC directory, labeler code 12502

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

Cilag AG (labeler code 12502) lists 7 products in the FDA National Drug Code Directory. By type: 6 bulk ingredients, 1 drugs for further processing. Its main marketing category is bulk ingredients. The newest product started marketing on January 21, 2021.

The request: Watch Cilag AG (FDA labeler code 12502): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
12502
Products in commercial distribution
7
Packages
8
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Controlled substance products
Schedule II 1
Started marketing in the last 12 months
0
Earliest marketing start
January 14, 2010
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients685.7%
Drugs for further processing114.3%

Products by type

TypeProductsShare
Bulk ingredients685.7%
Drugs for further processing114.3%

Dosage forms

Dosage formProductsShare
Powder685.7%
Injection, suspension114.3%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Rilpivirine hydrochloride12502-5500Injection, suspensionDrugs for further processingJanuary 21, 2021
Erdafitinib12502-6848PowderBulk ingredientsDecember 4, 2019
Remifentanil hydrochloride12502-5343PowderBulk ingredientsDecember 13, 2013
Cladribine12502-5406PowderBulk ingredientsAugust 1, 2010
Bortezomib12502-5268PowderBulk ingredientsAugust 1, 2010
Cladribine12502-4912PowderBulk ingredientsAugust 1, 2010
Alcaftadine12502-5263PowderBulk ingredientsJanuary 14, 2010

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.