RABBIT .1 g/mL
RABBIT · INJECTION, SOLUTION · ALK-Abello, Inc.
Rabbit is an over-the-counter injectable solution administered under the skin. The specific medical use or drug class for this product is not clearly documented in standard references.
Key Facts
- Brand Name
- RABBIT
- Generic Name
- RABBIT
- NDC Code (Product)
0268-0650- Manufacturer
- ALK-Abello, Inc.
- Strength
- .1 g/mL
- Dosage Form
- INJECTION, SOLUTION
- Route
- SUBCUTANEOUS
- Marketing Status
- Application #
- BLA103753
- Marketing Start
- 01/01/1965
Recall History
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.
Frequently Asked Questions
What is RABBIT used for?
Rabbit is an over-the-counter injectable solution administered under the skin. The specific medical use or drug class for this product is not clearly documented in standard references.
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 .1 g/mL?
The NDC (National Drug Code) for RABBIT .1 g/mL is 0268-0650, listed by ALK-Abello, Inc..
Other RABBIT Dosages
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)