TUNA .1 g/mL
THUNNUS THYNNUS · INJECTION, SOLUTION · ALK-Abello, Inc.
No Recall History
Plain English
TUNA is a injection, solution containing thunnus thynnus at .1 g/mL, taken percutaneous. Manufactured by ALK-Abello, Inc..
Key Facts
- Brand Name
- TUNA
- Generic Name
- THUNNUS THYNNUS
- NDC Code (Product)
0268-6226- Manufacturer
- ALK-Abello, Inc.
- Strength
- .1 g/mL
- Dosage Form
- INJECTION, SOLUTION
- Route
- PERCUTANEOUS
- Marketing Status
- Application #
- BLA103753
- Marketing Start
- 02/23/1998
Recall History
No Recall HistoryFrequently Asked Questions
What is TUNA used for?
TUNA contains THUNNUS THYNNUS. It is a injection, solution taken percutaneous. Consult your doctor for specific uses.
Is TUNA a controlled substance?
TUNA is not classified as a controlled substance by the DEA.
What is the generic name for TUNA?
The generic name for TUNA is THUNNUS THYNNUS. There are no other listed brand versions of THUNNUS THYNNUS.
What is the NDC code for TUNA .1 g/mL?
The NDC (National Drug Code) for TUNA .1 g/mL is 0268-6226, listed by ALK-Abello, Inc..
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)