FDAFDA · Food and drugs·Recall number D-0897-2017
Acyclovir Tablets, USP, 800 mg, 100-count bottle, Rx Only, Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ 08854, by Hetero Labs Limited, Unit V, Polepally, Jadcherla, Mahaboob Nagar - 509 301, India, NDC 31722-778-01
Published June 14, 2017 · Recall initiated: April 27, 2017
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Presence of Foreign Substance: human hair melded into tablet.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- ACYCLOVIR
- Manufacturer
- Hetero USA Inc
- Distributor
- Nationwide
- UPC
- 0331722777018
- Lot
- Lot # ACY16075 Exp. 09/2018
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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