NDC 0185-0122
Nitrofurantoin (monohydrate/macrocrystals) 25 mg / 75 mg capsule
On the label: Sandoz 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 Sandoz Inc. names for other drugs.
Recalls
- Nov 2, 2018 · Class III · Sandoz Inc
Cross Contamination with Other Products
Lots: Lots: a) JB4952, JA7322 Exp. 03/2020; b) JA7324, Exp.03/2020
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Nitrofurantoin: every company that makes it
- Form
- capsule, oral
- Strength
- 25 mg / 75 mg
- Approval
- ANDA ANDA077066
- On the market since
- Apr 6, 2005
- Package NDCs
0185-0122-010185-0122-10- Official label
- DailyMed (National Library of Medicine), updated Feb 28, 2024
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