Budesonide
- Product NDC
- 68788-6873
- 11-digit product format
- 687886873
- Labeler code
- 68788
- Product ID
- 68788-6873_4d77fbef-7c20-4fac-b629-f93b66305c2c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- BUDESONIDE
- Dosage form
- INHALANT
- Route
- RESPIRATORY (INHALATION)
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA078202
- Marketing category
- ANDA
- Marketing start
- 2017-01-20
- Marketing end
- 0000-00-00
- Substance
- BUDESONIDE
- Active strength
- 1 mg/2mL
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record