NDC 16714-439
Nitrofurantoin (monohydrate/macrocrystals) 25 mg / 75 mg capsule
On the label: Northstar Rx LLC..
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 Northstar Rx LLC. names for other drugs.
Recalls
- Nov 2, 2018 · Class III · Sandoz Inc
Cross Contamination with Other Products
Lots: Lot #: JA7319, JA 7320, JA7321, 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
- Strength
- 25 mg / 75 mg
- Approval
- ANDA ANDA077066
- On the market since
- Nov 1, 2014
- Package NDCs
16714-439-0116714-439-02- Official label
- DailyMed (National Library of Medicine), updated Nov 30, 2021
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?