NDC 0143-9299
Ganciclovir 50 mg per 1 mL injection, powder, lyophilized, for solution
On the label: Hikma Pharmaceuticals USA Inc..
Where it's 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 Hikma Pharmaceuticals USA Inc. names for other drugs.
Recalls
- Dec 16, 2022 · Class II · Hikma Pharmaceuticals USA Inc.
Labeling: Label mix-up - one vial was mislabeled as Cladribine Injection 10mg/mL inside a 10-count carton of Ganciclovir 500 mg.
Lots: Lot#: BQ0006, Exp 08/2023
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Ganciclovir: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 50 mg per 1 mL
- Approval
- ANDA ANDA076222
- On the market since
- Jun 17, 2021
- Package NDCs
0143-9299-010143-9299-10- Official label
- DailyMed (National Library of Medicine), updated Feb 7, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?