voriconazole 200 mg/1
voriconazole · TABLET, FILM COATED · Bryant Ranch Prepack
voriconazole is a tablet, film coated containing voriconazole at 200 mg/1, taken oral. Manufactured by Bryant Ranch Prepack.
Key Facts
- Brand Name
- voriconazole
- Generic Name
- voriconazole
- NDC Code (Product)
71335-2911- Manufacturer
- Bryant Ranch Prepack
- Strength
- 200 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA200265
- Drug Class
- Azole Antifungal [EPC]
- Marketing Start
- 12/12/2011
Recall History
Martin Avenue Pharmacy, Inc.
Lack of Assurance of Sterility: Martin Avenue Pharmacy, Inc. is conducting a voluntary recall of all compounded sterile preparations within expiry. The recall is being initiated in connection with a recent FDA inspection due to observations associated with certain quality control procedures that present a risk to sterility assurance.
Pharmacy Innovations
Lack of Assurance of Sterility: FDA inspection revealed insanitary conditions at the facility.
Franck's Lab Inc., d.b.a. Franck's Compounding Lab
Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all Sterile Human Drugs distributed between 11/21/2011 and 05/21/2012. FDA environmental sampling revealed the presence of microorganisms and fungal growth in the clean room where sterile products were prepared.
US Compounding Inc
Lack of Assurance of Sterility; The firm is recalling all sterile preparations that are within expiry due to deficient practices which may have an impact on sterility assurance.
Glenmark Pharmaceuticals Inc., USA
CGMP Deviations
Natures Pharmacy & Compounding Center
Lack of Sterility Assurance: All lots of sterile products compounded by the pharmacy that are not expired due to concerns associated with quality control procedures that present a potential risk to sterility assurance that were observed during a recent FDA inspection.
Pharmacy Plus, Inc. dba Vital Care Compounder
Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.
Attix Pharmaceuticals
Penicillin Cross Contamination: All lots of all products repackaged and distributed between 01/05/12 and 02/12/15 are being recalled because they were repackaged in a facility with penicillin products without adequate separation which could introduce the potential for cross contamination with penicillin.
Natures Pharmacy & Compounding Center
Lack of Sterility Assurance: All lots of sterile products compounded by the pharmacy that are not expired due to concerns associated with quality control procedures that present a potential risk to sterility assurance that were observed during a recent FDA inspection.
Amerisource Health Services LLC
cGMP Deviations: Received notification from their supplier requesting they perform a recall due to the fact they repackaged the product.
Frequently Asked Questions
What is voriconazole used for?
voriconazole contains voriconazole. It is a tablet, film coated taken oral. Consult your doctor for specific uses.
Is voriconazole a controlled substance?
voriconazole is not classified as a controlled substance by the DEA.
What is the generic name for voriconazole?
The generic name for voriconazole is voriconazole. There are 9 other brand versions of voriconazole.
What is the NDC code for voriconazole 200 mg/1?
The NDC (National Drug Code) for voriconazole 200 mg/1 is 71335-2911, listed by Bryant Ranch Prepack.