THUNNUS THYNNUS

FDA Drug Profile — TUNA

Drug Details

Generic Name
THUNNUS THYNNUS
Brand Names
TUNA
Application Number
BLA103753
Sponsor
ALK-Abello, Inc.
NDC Codes
1
Dosage Forms
INJECTION, SOLUTION
Routes
PERCUTANEOUS
Active Ingredients
NORTHERN BLUEFIN TUNA

Indications and Usage

USES: For temporary relief of gastrointestinal dyspepsia with flatulence and bloating, loss of weight and intolerance of certain foods.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Warnings

WARNINGS: If pregnant or breast-feeding, ask a health care professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.