Class III · Low risk
Nitrofurantoin Monohydrate/Macrocrystals capsules
Cross contamination with other products: Product is being recalled due to the potential presence of unrelated ingredients (Benazepril, Haloperidol and Perphenazine).
National Drug Code
Is NDC 0185-0122 recalled?
Nitrofurantoin (monohydrate/macrocrystals)
This product was recalled — in other package sizes
No FDA recall names your exact package code, but 2 recalls cover the same product (0185-0122) in a different bottle or carton size. Worth checking with your pharmacist.
- Active ingredient
- Nitrofurantoin (monohydrate/macrocrystals)
- Strength
- NITROFURANTOIN MONOHYDRATE 75 mg/1; NITROFURANTOIN 25 mg/1
- Form
- Capsule · Oral
- Labeler
- Sandoz Inc
- Type
- Human Prescription Drug
- Product code
- 0185-0122
Recalls of this product
Class III · Low risk
Nitrofurantoin Capsules
Cross Contamination with Other Products
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
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.