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Data / Drug companies / BTG International Inc.

BTG International Inc.: 10 products in the FDA NDC directory, labeler code 50633

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

BTG International Inc. (labeler code 50633) lists 10 products in the FDA National Drug Code Directory, covering 8 finished drugs by generic name. By type: 6 prescription drugs, 2 plasma derivatives. Its main marketing category is new drug applications (NDA). The newest product started marketing on September 1, 2026.

The request: Watch BTG International Inc. (FDA labeler code 50633): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
50633
Products in commercial distribution
10
Packages
11
Finished drugs by generic name
8
Prescription products
6
Over the counter products
2
Flagged as original packager
8 of 8 products that carry the flag
Started marketing in the last 12 months
2
Products with a marketing end date set
1
Earliest marketing start
October 2, 2000
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)440%
Biologics (BLA)440%
Generic drugs (ANDA)220%

Products by type

TypeProductsShare
Prescription drugs660%
Plasma derivatives220%
Over the counter drugs220%

Drugs it lists

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

DrugProductsCompanies listing it
Potassium iodide210
Uridine triacetate21
Hydroxocobalamin13
Ovine digoxin immune fab12
Ovine crotalidae venoms immune fab11
Naxitamab11
Glucarpidase11
Iloprost11

Dosage forms

Dosage formProductsShare
Injection, powder, lyophilized, for solution330%
Tablet220%
Granule220%
Injection110%
Injection, powder, for solution110%
Injection, solution110%

Pharmacologic classes

FDA established pharmacologic classes of its products.

ClassProducts
Pyrimidine Analog2
Antidote1
Cardiac Glycoside1
Antivenin1
Glycolipid Disialoganglioside-directed Antibody1
Carboxypeptidase1
Prostacycline1

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Danyelza50633-230InjectionBiologics (BLA)September 1, 2026
Thyrosafe50633-920TabletGeneric drugs (ANDA)November 26, 2025
Aurlumyn50633-340Injection, solutionNew drug applications (NDA)August 1, 2025
Vistogard50633-220GranuleNew drug applications (NDA)July 31, 2024
Xuriden50633-330GranuleNew drug applications (NDA)May 31, 2024
Cyanokit50633-310Injection, powder, lyophilized, for solutionNew drug applications (NDA)December 15, 2021
Voraxaze50633-210Injection, powder, for solutionBiologics (BLA)April 1, 2012
ThyroSafe50633-910TabletGeneric drugs (ANDA)September 30, 2002
DigiFab50633-120Injection, powder, lyophilized, for solutionBiologics (BLA)August 31, 2001
CroFab50633-110Injection, powder, lyophilized, for solutionBiologics (BLA)October 2, 2000

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.