Class II ยท Moderate risk
MISOPROSTOL Tablet
Labeling: Label Mixup; MISOPROSTOL Tablet, 100 mcg may be potentially mislabeled as QUINAPRIL HCL, Tablet, 10 mg, NDC 59762502001, Pedigree: AD42611_4, EXP: 5/14/2014.
National Drug Code
Is NDC 43386-0160-12 recalled?
Misoprostol · 120 TABLET in 1 BOTTLE (43386-160-12)
Yes — this exact package was recalled
1 FDA recall names the code 43386-0160-12 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
- Misoprostol
- Strength
- MISOPROSTOL 100 ug/1
- Form
- Tablet · Oral
- Labeler
- Lupin Pharmaceuticals,Inc.
- Type
- Human Prescription Drug
- Product code
- 43386-0160
Recalls naming this package
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
- 43386-0450 Nitrofurantoin 2
- 43386-0541 Morphine Sulfate 2
- 43386-0038 Voriconazole 1
- 43386-0050 Gavilyte-N 1
Free recall alerts
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