ENTACAPONE 200 mg/1
ENTACAPONE · TABLET, FILM COATED · Alembic Pharmaceuticals Limited
No Recall History
Plain English
ENTACAPONE is a tablet, film coated containing entacapone at 200 mg/1, taken oral. Manufactured by Alembic Pharmaceuticals Limited.
Key Facts
- Brand Name
- ENTACAPONE
- Generic Name
- ENTACAPONE
- NDC Code (Product)
46708-478- Manufacturer
- Alembic Pharmaceuticals Limited
- Strength
- 200 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA212601
- Drug Class
- Catechol-O-Methyltransferase Inhibitor [EPC]
- Marketing Start
- 01/06/2022
Recall History
No Recall HistorySide Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
hallucination530 reports
fall523 reports
dyskinesia496 reports
death383 reports
drug ineffective379 reports
parkinson^s disease317 reports
confusional state282 reports
gait disturbance276 reports
tremor270 reports
on and off phenomenon250 reports
Frequently Asked Questions
What is ENTACAPONE used for?
ENTACAPONE contains ENTACAPONE. It is a tablet, film coated taken oral. Consult your doctor for specific uses.
Is ENTACAPONE a controlled substance?
ENTACAPONE is not classified as a controlled substance by the DEA.
What is the generic name for ENTACAPONE?
The generic name for ENTACAPONE is ENTACAPONE. There are 11 other brand versions of ENTACAPONE.
What is the NDC code for ENTACAPONE 200 mg/1?
The NDC (National Drug Code) for ENTACAPONE 200 mg/1 is 46708-478, listed by Alembic Pharmaceuticals Limited.