NDC 67296-2127
Valacyclovir Hydrochloride 500 mg tablet, film coated
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Mylan Pharmaceuticals Inc.'s NDC 0378-4275.
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 Mylan Pharmaceuticals Inc. names for other drugs.
Repackaging site
- RedPharm Drug, Eden Prairie, MN, United States · repackages it
Recalls
- Apr 25, 2024 · Class III · Viatris Inc
Failed Tablet/Capsule Specifications: There is a potential for the imprint, M 122, to be missing on some tablets.
Lots: Lot #: 3183269, Exp. Date May 2025; 3157326, Exp. date June 2024
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, film coated, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA078518
- On the market since
- May 24, 2010
- Package NDCs
67296-2127-2- Official label
- DailyMed (National Library of Medicine), updated Dec 23, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?