Budesonide
- Product NDC
- 68788-7020
- 11-digit product format
- 687887020
- Labeler code
- 68788
- Product ID
- 68788-7020_8b6a5c2b-4160-443d-bb2d-fb60cda00d42
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Budesonide
- Dosage form
- SUSPENSION
- Route
- RESPIRATORY (INHALATION)
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA201966
- Marketing category
- ANDA
- Marketing start
- 2017-10-11
- Marketing end
- 0000-00-00
- Substance
- BUDESONIDE
- Active strength
- 0 mg/2mL
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record