NDC 0143-9342
Gemcitabine 38 mg per 1 mL injection, 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
- Jun 10, 2026 · Class II · McKesson
Temperature Abuse: Product was stored incorrectly in a controlled room temperature environment instead of a refrigerated environment.
Lots: Lot #: CB0046, Exp. Date 06/2027
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Gemcitabine: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 38 mg per 1 mL
- Approval
- ANDA ANDA213175
- On the market since
- Oct 17, 2025
- Package NDCs
0143-9342-01- Official label
- DailyMed (National Library of Medicine), updated Oct 24, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?