Class II · Moderate risk
Nitrofurantoin Oral Suspension
Subpotent Drug: Expansion of June 2018 recall of lots S700065 and S700619 due to below specification results for assay.
National Drug Code
Is NDC 43386-0450-11 recalled?
Nitrofurantoin · 1 BOTTLE in 1 CARTON (43386-450-11) / 230 mL in 1 BOTTLE
Yes — this exact package was recalled
2 FDA recalls name the code 43386-0450-11 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
- Nitrofurantoin
- Strength
- NITROFURANTOIN 25 mg/5mL
- Form
- Suspension · Oral
- Labeler
- Lupin Pharmaceuticals,Inc.
- Type
- Human Prescription Drug
- Product code
- 43386-0450
Recalls naming this package
Class II · Moderate risk
Nitrofurantoin Oral Suspension USP
Subpotent Drug and Failed Content Uniformity.
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
- 43386-0069 Fluocinolone Acetonide 3
- 43386-0060 GaviLyte - C TM 2
- 43386-0541 Morphine Sulfate 2
- 43386-0038 Voriconazole 1
- 43386-0050 Gavilyte-N 1
- 43386-0118 Hydrocodone Bitartrate and Homatropine Methylbromide 1
Free recall alerts
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