Tobacco Leaf

FDA Drug Profile — Tobacco Leaf

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

Drug Details

Generic Name
Tobacco Leaf
Brand Names
Tobacco Leaf
Application Number
BLA102211
Sponsor
Allermed Laboratories, Inc.
NDC Codes
1
Dosage Forms
INJECTION
Routes
CUTANEOUS, INTRADERMAL, SUBCUTANEOUS
Active Ingredients
TOBACCO LEAF

Indications and Usage

Take 15 minutes before meals

Warnings

WARNINGS Stop use and ask doctor if symptoms persist more than 5 days. If pregnant or breast-feeding 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 ethyl alcohol 30%