Borrelia Burgdorferi

FDA Drug Profile — Borrelia Burgdorferi

Borrelia Burgdorferi is listed in the FDA National Drug Code directory with 1 NDC code, marketed under brand name including Borrelia Burgdorferi. Available dosage form: liquid.

Drug Details

Generic Name
Borrelia Burgdorferi
Brand Names
Borrelia Burgdorferi
Application Number
Sponsor
Newton Laboratories, Inc.
NDC Codes
1
Dosage Forms
LIQUID
Routes
ORAL
Active Ingredients
BORRELIA BURGDORFERI

Indications and Usage

INDICATIONS: For temporary relief of aches and pains of joints and muscles as a consequence of infection.

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.