The care inside an online program
U.S. care · September 2026.
Know what a source can actually settle.
A drug record, a state record, and a warning letter each answer a different question. Use the notes below to see what each can tell you.
The agency that reviews drug products is the Food and Drug Administration, or FDA.
Approval belongs to the exact product
The National Drug Code Directory is FDA’s list of drug products and their identifying codes.
As of September 2026, being in this list did not mean FDA had approved a medicine.
Each listed product has an identifying code, often called an NDC number.
A product’s code is not an approval decision.
Find the exact drug name and check whether it is taken as a pill, a shot, or another form.
Also check what illness FDA approved that product to treat.
Note AA licence record answers who may practise
A state medical board is the state body that gives doctors permission to practise medicine and can take action against them.
Records checked in September 2026 showed whether a doctor had a licence and any public penalties or accusations of breaking the medical board’s rules.
A “clean” record means it shows no public penalty or formal accusation from the medical board.
It does not rate the quality of the doctor’s care.
The Federation of State Medical Boards has a state-board directory, checked in September 2026.
Note BNote CA pharmacy record is a separate check
State pharmacy boards give pharmacies permission to operate.
FDA linked to these state licence searches in information checked in September 2026.
Use the pharmacy’s name, then match the licence record to the name you were given.
Note DA warning letter raises concerns at a point in time
As of September 2026, FDA warned that later contact with a company could change the concerns raised in its warning letter.
A warning letter says FDA believes a company has broken a rule.
It is not a final decision by a court.
If no letter is listed, the company may simply never have been reviewed.
Note EA report does not prove a drug caused harm
FDA’s public reports can flag a problem, but do not prove the drug caused it, under guidance checked in September 2026.
These reports cannot tell you how often the problem happens.
That limits what a list of reports can tell you about your own chance of a problem.
Note FNotes for this page
- AFDA: product codes and the drug directory
- BFind your state’s medical board
- CMedical boards: public licence records
- DFDA: state pharmacy licence searches
- EFDA: the agency’s letter search
- FFDA: limits of medicine-problem reports