ZELAPAR 1.25 mg/1
SELEGILINE HYDROCHLORIDE · TABLET, ORALLY DISINTEGRATING · Bausch Health US, LLC
ZELAPAR is a tablet, orally disintegrating containing selegiline hydrochloride at 1.25 mg/1, taken oral. Manufactured by Bausch Health US, LLC.
Key Facts
- Brand Name
- ZELAPAR
- Generic Name
- SELEGILINE HYDROCHLORIDE
- NDC Code (Product)
0187-0453- Manufacturer
- Bausch Health US, LLC
- Strength
- 1.25 mg/1
- Dosage Form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Marketing Status
- Application #
- NDA021479
- Marketing Start
- 06/14/2006
Recall History
No Recall HistoryFrequently Asked Questions
What is ZELAPAR used for?
ZELAPAR contains SELEGILINE HYDROCHLORIDE. It is a tablet, orally disintegrating taken oral. Consult your doctor for specific uses.
Is ZELAPAR a controlled substance?
ZELAPAR is not classified as a controlled substance by the DEA.
What is the generic name for ZELAPAR?
The generic name for ZELAPAR is SELEGILINE HYDROCHLORIDE. There are 11 other brand versions of SELEGILINE HYDROCHLORIDE.
What is the NDC code for ZELAPAR 1.25 mg/1?
The NDC (National Drug Code) for ZELAPAR 1.25 mg/1 is 0187-0453, listed by Bausch Health US, LLC.
Other Selegiline Brands
See all →- Selegiline Hydrochloride5 mg/150090-2918
- SELEGILINE HYDROCHLORIDE5 mg/160505-0055
- Selegiline Hydrochloride5 mg/171335-2673
- Selegiline Hydrochloride5 mg/160505-3438
- Selegiline Hydrochloride5 mg/171205-888
- Selegiline Hydrochloride5 mg/116571-659
- Selegiline Hydrochloride5 mg/162135-694
- Selegiline Hydrochloride5 mg/160429-176
- Selegiline Hydrochloride5 mg/171335-2676
- Selegiline Hydrochloride5 mg/170954-504
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)