Azurity Pharmaceuticals, Inc
Azurity Pharmaceuticals, Inc is listed as the manufacturer on 1 FDA drug label records covering 1 distinct active ingredients predominantly human prescription drug products.
About Azurity Pharmaceuticals, Inc
Azurity Pharmaceuticals, Inc is named as the labeler on 1 FDA drug label records. Its catalogue spans 1 distinct active ingredients, led by VANCOMYCIN HYDROCHLORIDE. Most of these labels are human prescription drug products. Labelling across this portfolio most often references: pediatric patients, years age, treatment clostridium, associated diarrhea, enterocolitis caused, staphylococcus aureus, including methicillin, resistant strains. Use the table below to identify a specific product, then open it for full indications, dosage and warnings as filed with the FDA.
Active ingredients in this portfolio
| Active ingredient | Products |
|---|---|
| VANCOMYCIN HYDROCHLORIDE | 1 |
FDA drug products from Azurity Pharmaceuticals, Inc
| Brand name | Generic | Type | Route |
|---|---|---|---|
| FIRVANQ | VANCOMYCIN HYDROCHLORIDE | HUMAN PRESCRIPTION DRUG |
Frequently asked questions
How many FDA drug products does Azurity Pharmaceuticals, Inc make?
1 FDA drug label records name Azurity Pharmaceuticals, Inc as the manufacturer, covering 1 distinct active ingredients.
What active ingredients does Azurity Pharmaceuticals, Inc produce?
The most frequent active ingredients in this portfolio are VANCOMYCIN HYDROCHLORIDE.
Are Azurity Pharmaceuticals, Inc products prescription or over-the-counter?
The largest share of this company’s labels are human prescription drug products; check each product page for its own marketing status.
Does this page list prices or where to buy?
No. This is a labelling reference built from FDA data. It does not sell, price or recommend any medicine.
Labelling data reproduced from FDA Structured Product Labelling for identification only. This site does not sell, price or recommend any medicine.