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Data / Drug companies / Swiss Caps AG

Swiss Caps AG: 6 products in the FDA NDC directory, labeler code 65655

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

Swiss Caps AG (labeler code 65655) lists 6 products in the FDA National Drug Code Directory. By type: 6 drugs for further processing. Its main marketing category is drugs for further processing. The newest product started marketing on August 26, 2015.

The request: Watch Swiss Caps AG (FDA labeler code 65655): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
65655
Products in commercial distribution
6
Packages
6
Finished drugs by generic name
0
Prescription products
0
Over the counter products
0
Started marketing in the last 12 months
0
Earliest marketing start
April 16, 1996
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Drugs for further processing6100%

Products by type

TypeProductsShare
Drugs for further processing6100%

Dosage forms

Dosage formProductsShare
Capsule, liquid filled466.7%
Suppository233.3%

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Isotretinoin65655-0005Capsule, liquid filledDrugs for further processingAugust 26, 2015
Isotretinoin65655-0006Capsule, liquid filledDrugs for further processingMay 1, 2012
Isotretinoin65655-0004Capsule, liquid filledDrugs for further processingMay 1, 2012
Isotretinoin65655-0003Capsule, liquid filledDrugs for further processingMay 1, 2012
Miconazole nitrate65655-0013SuppositoryDrugs for further processingJune 29, 2001
Miconazole nitrate65655-0014SuppositoryDrugs for further processingApril 16, 1996

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.