Class II ยท Moderate risk
Acyclovir Tablets USP 800 mg
Presence of Particulate Matter: Product from lot KF2199, may contain tablets with pieces of nitrile rubber glove embedded within the tablets.
National Drug Code
Is NDC 60505-5307-01 recalled?
acyclovir · 100 TABLET in 1 BOTTLE (60505-5307-1)
Yes — this exact package was recalled
1 FDA recall names the code 60505-5307-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- acyclovir
- Strength
- ACYCLOVIR 800 mg/1
- Form
- Tablet · Oral
- Labeler
- Apotex Corp.
- Type
- Human Prescription Drug
- Product code
- 60505-5307
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 60505-0589 Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution 3
- 60505-0829 Fluticasone Propionate 3
- 60505-2580 Atorvastatin Calcium 3
- 60505-0595 See recall 2
- 60505-0596 See recall 2
- 60505-0773 See recall 2
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.