Class II ยท Moderate risk
Mirtazapine Tablets
Presence of Foreign Tablets/Capsules; possibility of Glipizide 10 mg tablets commingled
National Drug Code
Is NDC 51079-0088-20 recalled?
Mirtazapine · 100 BLISTER PACK in 1 CARTON (51079-088-20) / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-088-01)
Yes — this exact package was recalled
1 FDA recall names the code 51079-0088-20 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
- Mirtazapine
- Strength
- MIRTAZAPINE 45 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Mylan Institutional Inc.
- Type
- Human Prescription Drug
- Product code
- 51079-0088
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
- 51079-0443 Levothyroxine Sodium 2
- 51079-0445 Levothyroxine Sodium 2
- 51079-0881 See recall 2
- 51079-0947 See recall 2
- 51079-0020 See recall 1
- 51079-0090 See recall 1
Free recall alerts
Know the day your medication is recalled
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