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Data / Drug companies / Agc Pharma Chemicals Europe, S.l.u.

Agc Pharma Chemicals Europe, S.l.u.: 8 products in the FDA NDC directory, labeler code 65404

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

Agc Pharma Chemicals Europe, S.l.u. (labeler code 65404) lists 8 products in the FDA National Drug Code Directory. By type: 8 bulk ingredients. Its main marketing category is bulk ingredients for compounding. The newest product started marketing on October 1, 2026.

The request: Watch Agc Pharma Chemicals Europe, S.l.u. (FDA labeler code 65404): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
65404
Products in commercial distribution
8
Packages
8
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Started marketing in the last 12 months
3
Earliest marketing start
January 1, 1999
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Bulk ingredients for compounding675%
Bulk ingredients225%

Products by type

TypeProductsShare
Bulk ingredients8100%

Dosage forms

Dosage formProductsShare
Powder787.5%
Capsule112.5%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Zongertinib65404-011PowderBulk ingredients for compoundingOctober 1, 2026
Taletrectinib adipate65404-010PowderBulk ingredients for compoundingJune 1, 2026
Taletrectinib adipate65404-009CapsuleBulk ingredients for compoundingJune 1, 2026
Dapiprazole hydrochloride65404-008PowderBulk ingredients for compoundingJune 30, 2024
Pimobendan65404-004PowderBulk ingredientsFebruary 17, 2016
Telmisartan65404-007PowderBulk ingredients for compoundingJanuary 1, 2004
Telmisartan65404-006PowderBulk ingredientsJanuary 1, 2004
Dipyridamole65404-005PowderBulk ingredients for compoundingJanuary 1, 1999

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.