NDC 53002-0640
Famciclovir 250 mg tablet, film coated
On the label: RPK Pharmaceuticals, Inc.. It's repackaged: RPK Pharmaceuticals, Inc. rebottles it from Camber Pharmaceuticals Inc.'s NDC 31722-707.
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 Camber Pharmaceuticals Inc. names for other drugs.
Repackaging site
- RPK Pharmaceuticals, Inc., Union City, California, United States · repackages it and relabels it
Recalls
- Dec 22, 2017 · Class II · Hetero Labs Limited Unit V
Temperature Abuse: Complaints of tablets being wet and stuck together with tablet coating peeled and disintegrated as a result of prolonged exposure to high temp during distribution.
Lots: Lot # FMC17039, Exp 07/2019.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Penciclovir: every company that makes it
- Form
- tablet, film coated
- Strength
- 250 mg
- Approval
- ANDA ANDA202438
- On the market since
- Sep 10, 2014
- Package NDCs
53002-0640-253002-0640-3- Official label
- DailyMed (National Library of Medicine), updated Aug 10, 2023
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?