ALMOND .1 g/mL
PRUNUS DULCIS · INJECTION, SOLUTION · ALK-Abello, Inc.
No Recall History
Plain English
ALMOND is a injection, solution containing prunus dulcis at .1 g/mL, taken percutaneous. Manufactured by ALK-Abello, Inc..
Key Facts
- Brand Name
- ALMOND
- Generic Name
- PRUNUS DULCIS
- NDC Code (Product)
0268-6100- Manufacturer
- ALK-Abello, Inc.
- Strength
- .1 g/mL
- Dosage Form
- INJECTION, SOLUTION
- Route
- PERCUTANEOUS
- Marketing Status
- Application #
- BLA103753
- Marketing Start
- 02/23/1998
Recall History
No Recall HistorySide Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
toxicity to various agents5,899 reports
completed suicide5,392 reports
drug abuse5,245 reports
overdose1,891 reports
death1,628 reports
intentional overdose1,524 reports
cardio-respiratory arrest1,344 reports
suicide attempt1,323 reports
somnolence928 reports
drug dependence915 reports
Frequently Asked Questions
What is ALMOND used for?
ALMOND contains PRUNUS DULCIS. It is a injection, solution taken percutaneous. Consult your doctor for specific uses.
Is ALMOND a controlled substance?
ALMOND is not classified as a controlled substance by the DEA.
What is the generic name for ALMOND?
The generic name for ALMOND is PRUNUS DULCIS. There are 2 other brand versions of PRUNUS DULCIS.
What is the NDC code for ALMOND .1 g/mL?
The NDC (National Drug Code) for ALMOND .1 g/mL is 0268-6100, listed by ALK-Abello, Inc..