NDC 71205-391
acyclovir 400 mg tablet
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Apotex Corp.'s NDC 60505-5306.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Apotex Corp. names for other drugs.
Repackaging site
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels it
Recalls
- Jul 17, 2013 · Class II · Apotex Inc.
Presence of Particulate Matter: Product from lot KF2199, may contain tablets with pieces of nitrile rubber glove embedded within the tablets.
Lots: Lot # KF2199 Exp 07/15
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Acyclovir: every company that makes it
- Form
- tablet, oral
- Strength
- 400 mg
- Approval
- ANDA ANDA077309
- On the market since
- Jun 9, 2007
- Package NDCs
71205-391-2571205-391-3071205-391-6071205-391-90- Official label
- DailyMed (National Library of Medicine), updated Feb 1, 2020
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?