Carbidopa 25 mg/1
Carbidopa Tablets · TABLET · Oceanside Pharmaceuticals
No Recall History
Plain English
Carbidopa is a tablet containing carbidopa tablets at 25 mg/1, taken oral. Manufactured by Oceanside Pharmaceuticals.
Key Facts
- Brand Name
- Carbidopa
- Generic Name
- Carbidopa Tablets
- NDC Code (Product)
68682-200- Manufacturer
- Oceanside Pharmaceuticals
- Strength
- 25 mg/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- Application #
- NDA017830
- Drug Class
- Aromatic Amino Acid Decarboxylation Inhibitor [EPC]
- Marketing Start
- 04/04/2014
Recall History
No Recall HistoryFrequently Asked Questions
What is Carbidopa used for?
Carbidopa contains Carbidopa Tablets. It is a tablet taken oral. Consult your doctor for specific uses.
Is Carbidopa a controlled substance?
Carbidopa is not classified as a controlled substance by the DEA.
What is the generic name for Carbidopa?
The generic name for Carbidopa is Carbidopa Tablets. There are no other listed brand versions of Carbidopa Tablets.
What is the NDC code for Carbidopa 25 mg/1?
The NDC (National Drug Code) for Carbidopa 25 mg/1 is 68682-200, listed by Oceanside Pharmaceuticals.
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)