Class III · Low risk
Norepinephrine Bitartrate Injection
Failed Impurities/Degradation Specifications: Above the specification limits yielded for related substance norepinephrine sulfonic acid impurity during routine product monitoring.
National Drug Code
Is NDC 47335-0615-40 recalled?
Norepinephrine Bitartrate
Yes — this exact package was recalled
1 FDA recall names the code 47335-0615-40 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
- Norepinephrine Bitartrate
- Strength
- NOREPINEPHRINE BITARTRATE 1 mg/mL
- Form
- Injection, Solution, Concentrate · Intravenous
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Type
- Human Prescription Drug
- Product code
- 47335-0615
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
- 47335-0737 Bupropion hydrochloride 6
- 47335-0738 Bupropion hydrochloride 5
- 47335-0506 Cequa 4
- 47335-0063 Dofetilide 2
- 47335-0343 See recall 2
- 47335-0049 Doxorubicin Hydrochloride 1
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