Alfalfa

FDA Drug Profile — MEDICAGO SATIVA POLLEN

Alfalfa is listed in the FDA National Drug Code directory with 4 NDC codes, marketed under brand name including MEDICAGO SATIVA POLLEN. Available dosage forms: powder, injection, solution.

Drug Details

Generic Name
Alfalfa
Brand Names
MEDICAGO SATIVA POLLEN
Application Number
BLA103753
Sponsor
Schwabe North America, Inc.
NDC Codes
4
Dosage Forms
POWDER, INJECTION, SOLUTION
Routes
PERCUTANEOUS, SUBCUTANEOUS
Active Ingredients
ALFALFA, MEDICAGO SATIVA POLLEN

Indications and Usage

Uses: For temporary relief of minor: fatigue* headache* muscle aches and cramps* irritability* water retention* sadness* *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Warnings

Warnings: If pregnant or breastfeeding , ask a health professional before use. Do not use if clear seal over the cap is broken or missing. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Stop use and ask a doctor if fatigue, headache, muscle aches and cramps, irritability, water retention, sadness, or other symptoms do not improve within 7 days or are accompanied by fever.