Drugplain

RABBIT .05 g/mL

RABBIT · INJECTION, SOLUTION · ALK-Abello, Inc.

1 Recall on Record
Plain English

Rabbit is an over-the-counter injectable solution administered under the skin. The drug class and specific therapeutic use are not currently specified in available information.

Key Facts

Brand Name
RABBIT
Generic Name
RABBIT
NDC Code (Product)
0268-0651
Manufacturer
ALK-Abello, Inc.
Strength
.05 g/mL
Dosage Form
INJECTION, SOLUTION
Route
SUBCUTANEOUS
Marketing Status
Application #
BLA103753
Marketing Start
01/01/1965

Recall History

1 Recall on Record
Class I08/12/2013

Jack Rabbit, Inc

Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the FDA has determined that J.R. Jack Rabbit Male Enhancement product was found to contain two undeclared active pharmaceutical ingredients: sildenafil and tadalafil.

TerminatedVoluntary: Firm initiated

Frequently Asked Questions

What is RABBIT used for?

Rabbit is an over-the-counter injectable solution administered under the skin. The drug class and specific therapeutic use are not currently specified in available information.

Is RABBIT a controlled substance?

RABBIT is not classified as a controlled substance by the DEA.

What is the generic name for RABBIT?

The generic name for RABBIT is RABBIT. There are no other listed brand versions of RABBIT.

What is the NDC code for RABBIT .05 g/mL?

The NDC (National Drug Code) for RABBIT .05 g/mL is 0268-0651, listed by ALK-Abello, Inc..

Product NDC

0268-0651

Package NDC

0268-0651-10

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)