Details for New Drug Application (NDA): 206623
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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
Mechanism of Action | Corticosteroid Hormone Receptor Agonists |
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: | RX | Dosage: | CAPSULE, DELAYED RELEASE;ORAL | Strength | 3MG | ||||
Approval Date: | Apr 8, 2016 | TE: | AB | RLD: | No |
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