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Last Updated: November 22, 2024

Details for New Drug Application (NDA): 206623


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NDA 206623 describes BUDESONIDE, which is a drug marketed by Padagis Israel, Amneal Pharms, Aurobindo Pharma Usa, Barr Labs Div Teva, Dr Reddys Labs Sa, Natco, Rising, Sciecure Pharma Inc, Zydus Pharms, Apotex Inc, Cipla, Eugia Pharma, Impax Labs Inc, Lupin, Nephron, Sandoz, Sun Pharm, Teva Pharms, Teva Pharms Usa, Actavis Labs Fl Inc, and Mylan, and is included in twenty-one NDAs. It is available from thirty-five suppliers. Additional details are available on the BUDESONIDE profile page.

The generic ingredient in BUDESONIDE is budesonide. There are twenty-two drug master file entries for this compound. Forty-three suppliers are listed for this compound. Additional details are available on the budesonide profile page.
Summary for 206623
Tradename:BUDESONIDE
Applicant:Dr Reddys Labs Sa
Ingredient:budesonide
Patents:0
Pharmacology for NDA: 206623
Medical Subject Heading (MeSH) Categories for 206623
Suppliers and Packaging for NDA: 206623
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
BUDESONIDE budesonide CAPSULE, DELAYED RELEASE;ORAL 206623 ANDA Golden State Medical Supply, Inc. 51407-128 51407-128-01 100 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51407-128-01)
BUDESONIDE budesonide CAPSULE, DELAYED RELEASE;ORAL 206623 ANDA Mayne Pharma Inc. 51862-580 51862-580-01 100 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51862-580-01)

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:CAPSULE, DELAYED RELEASE;ORALStrength3MG
Approval Date:Apr 8, 2016TE:ABRLD:No

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