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Data / Drug companies / Sebela Pharmaceuticals Inc.

Sebela Pharmaceuticals Inc.: 10 products in the FDA NDC directory, labeler code 54766

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

Sebela Pharmaceuticals Inc. (labeler code 54766) lists 10 products in the FDA National Drug Code Directory, covering 5 finished drugs by generic name. By type: 10 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on May 26, 2026.

The request: Watch Sebela Pharmaceuticals Inc. (FDA labeler code 54766): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
54766
Products in commercial distribution
10
Packages
9
Finished drugs by generic name
5
Prescription products
10
Over the counter products
0
Controlled substance products
Schedule IV 1
Flagged as original packager
10 of 10 products that carry the flag
Started marketing in the last 12 months
2
Products with a marketing end date set
6
Earliest marketing start
July 2, 2015
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
New drug applications (NDA)550%
Other unapproved drugs330%
Generic drugs (ANDA)220%

Products by type

TypeProductsShare
Prescription drugs10100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Tablet440%
Lotion220%
Ointment220%
Cream110%
Capsule110%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Pramosone54766-777OintmentOther unapproved drugsMay 26, 2026
Pramosone54766-763OintmentOther unapproved drugsMay 26, 2026
Imuran54766-590TabletNew drug applications (NDA)December 1, 2017
Motofen54766-200TabletNew drug applications (NDA)April 11, 2017
Ridaura54766-093CapsuleNew drug applications (NDA)December 15, 2016
Lotronex54766-895TabletNew drug applications (NDA)July 11, 2016
Lotronex54766-894TabletNew drug applications (NDA)July 11, 2016
Analpram HC54766-799CreamOther unapproved drugsAugust 7, 2015
Analpram HC54766-829LotionGeneric drugs (ANDA)August 5, 2015
Pramosone54766-729LotionGeneric drugs (ANDA)July 2, 2015

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.