BUDESONIDE 2 mg/1
budesonide · AEROSOL, FOAM · Padagis Israel Pharmaceuticals Ltd
No Recall History
Plain English
BUDESONIDE is a aerosol, foam containing budesonide at 2 mg/1, taken rectal. Manufactured by Padagis Israel Pharmaceuticals Ltd.
Key Facts
- Brand Name
- BUDESONIDE
- Generic Name
- budesonide
- NDC Code (Product)
45802-627- Manufacturer
- Padagis Israel Pharmaceuticals Ltd
- Strength
- 2 mg/1
- Dosage Form
- AEROSOL, FOAM
- Route
- RECTAL
- Marketing Status
- Application #
- ANDA215328
- Drug Class
- Corticosteroid [EPC]
- Marketing Start
- 04/17/2023
Recall History
No Recall HistoryFrequently Asked Questions
What is BUDESONIDE used for?
BUDESONIDE contains budesonide. It is a aerosol, foam taken rectal. Consult your doctor for specific uses.
Is BUDESONIDE a controlled substance?
BUDESONIDE is not classified as a controlled substance by the DEA.
What is the generic name for BUDESONIDE?
The generic name for BUDESONIDE is budesonide. There are 12 other brand versions of budesonide.
What is the NDC code for BUDESONIDE 2 mg/1?
The NDC (National Drug Code) for BUDESONIDE 2 mg/1 is 45802-627, listed by Padagis Israel Pharmaceuticals Ltd.
Other Budesonide Brands
See all →- Budesonide and formoterol fumarate dihydrate80 ug/10480-3080
- Budesonide32 ug/10536-1112
- budesonide3 mg/10574-9855
- Budesonide.25 mg/2mL47335-631
- SYMBICORT160 ug/150090-4509
- Budesonide Inhalation Suspension.5 mg/2mL68788-7314
- BREYNA160 ug/10378-7503
- budesonide3 mg/170771-1075
- Budesonide Inhalation.5 mg/2mL0115-1689
- PULMICORT RESPULES.25 mg/2mL0186-1988
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)