PROCYSBI 75 mg/1
Cysteamine bitartrate · GRANULE, DELAYED RELEASE · Horizon Therapeutics USA, Inc.
No Recall History
Plain English
PROCYSBI is a granule, delayed release containing cysteamine bitartrate at 75 mg/1, taken oral. Manufactured by Horizon Therapeutics USA, Inc..
Key Facts
- Brand Name
- PROCYSBI
- Generic Name
- Cysteamine bitartrate
- NDC Code (Product)
75987-140- Manufacturer
- Horizon Therapeutics USA, Inc.
- Strength
- 75 mg/1
- Dosage Form
- GRANULE, DELAYED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- NDA213491
- Marketing Start
- 02/14/2020
Recall History
No Recall HistoryFrequently Asked Questions
What is PROCYSBI used for?
PROCYSBI contains Cysteamine bitartrate. It is a granule, delayed release taken oral. Consult your doctor for specific uses.
Is PROCYSBI a controlled substance?
PROCYSBI is not classified as a controlled substance by the DEA.
What is the generic name for PROCYSBI?
The generic name for PROCYSBI is Cysteamine bitartrate. There are 2 other brand versions of Cysteamine bitartrate.
What is the NDC code for PROCYSBI 75 mg/1?
The NDC (National Drug Code) for PROCYSBI 75 mg/1 is 75987-140, listed by Horizon Therapeutics USA, Inc..