NDC 70518-1087
Nitrofurantoin (monohydrate/macrocrystals) 25 mg / 75 mg capsule
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Sandoz Inc.'s NDC 0185-0122.
Where the pills inside were 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 7, 2018 · Class III · RemedyRepack Inc.
Cross contamination with other products: Product is being recalled due to the potential presence of unrelated ingredients (Benazepril, Haloperidol and Perphenazine).
Lots: Lot #: B0484872-081718, B0481339-081018, Exp 08/2019; B0506246-092718, Exp 09/2019; B0509938-100418, Exp 10/2019 - 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
- Mar 29, 2018
- Package NDCs
70518-1087-070518-1087-170518-1087-270518-1087-3- Official label
- DailyMed (National Library of Medicine), updated Jul 2, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?