RABBIT

FDA Drug Profile — RABBIT

RABBIT is listed in the FDA National Drug Code directory with 2 NDC codes, marketed under brand name including RABBIT. Available dosage form: injection, solution.

Drug Details

Generic Name
RABBIT
Brand Names
RABBIT
Application Number
BLA103753
Sponsor
ALK-Abello, Inc.
NDC Codes
2
Dosage Forms
INJECTION, SOLUTION
Routes
SUBCUTANEOUS
Active Ingredients
RABBIT

Indications and Usage

Uses Helps promote and maintain normal metabolic functions. Directions To be taken 20 minutes away from food. Place drops directly under the tongue or into ¼ oz of water. Adults and adolescents (12 years and older): Take 10 drops two to three times daily or as recommended by your healthcare practitioner. Children (under 12 years): Take under the direction of your healthcare practitioner.

Warnings

Warnings Stop use and ask a doctor if symptoms persist or worsen. If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Contains: Shellfish (oyster)