Class III · Low risk
Bendamustine HCl Injection
Labeling: Missing Label; customer complaint received that labels were partially or completely peeled off injection vial.
National Drug Code
Is NDC 10019-0079-01 recalled?
Bendamustine Hydrochloride · 1 VIAL, MULTI-DOSE in 1 CARTON (10019-079-01) / 1 INJECTION in 1 VIAL, MULTI-DOSE
Yes — this exact package was recalled
1 FDA recall names the code 10019-0079-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- bendamustine hydrochloride
- Strength
- BENDAMUSTINE HYDROCHLORIDE 100 mg/1
- Form
- Injection · Intravenous
- Labeler
- Baxter Healthcare Corporation
- Type
- Human Prescription Drug
- Product code
- 10019-0079
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 10019-0055 Brevibloc 1
- 10019-0075 Brevibloc 1
- 10019-0553 See recall 1
- 10019-0651 Sevoflurane 1
Free recall alerts
Know the day your medication is recalled
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