Class I · High risk
NP Thyroid 30 Thyroid Tablets
Subpotent Drug
National Drug Code
Is NDC 42192-0329-01 recalled?
NP Thyroid 30 · 100 TABLET in 1 BOTTLE (42192-329-01)
Yes — this exact package was recalled
3 FDA recalls name the code 42192-0329-01 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
- Levothyroxine, Liothyronine
- Strength
- LEVOTHYROXINE 19 ug/1; LIOTHYRONINE 4.5 ug/1
- Form
- Tablet · Oral
- Labeler
- Acella Pharmaceuticals, LLC
- Type
- Human Prescription Drug
- Product code
- 42192-0329
Recalls naming this package
Class I · High risk
NP Thyroid 30
Superpotent Drug.
Class II · Moderate risk
LEVOTHYROXINE/ LIOTHYRONINE Tablet
Labeling: Label Mixup; LEVOTHYROXINE/ LIOTHYRONINE Tablet, 19 mcg/4.5 mcg may be potentially mislabeled as MAGNESIUM GLUCONATE DIHYDRATE, Tablet, 500 mg (27 mg Elemental Magnesium), NDC 60258017201, Pedigree: AD30197_16, EXP: 5/9/2014.
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
- 42192-0327 NP Thyroid 15 2
- 42192-0328 NP Thyroid 120 2
- 42192-0330 NP Thyroid 60 2
- 42192-0331 NP Thyroid 90 2
- 42192-0614 Phenytoin Sodium 2
- 42192-0113 See recall 1
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.