Class I · High risk
NP Thyroid 15 Thyroid Tablets
Subpotent Drug
National Drug Code
Is NDC 42192-0327-07 recalled?
NP Thyroid 15
Yes — this exact package was recalled
1 FDA recall names the code 42192-0327-07 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
- LIOTHYRONINE 2.25 ug/1; LEVOTHYROXINE 9.5 ug/1
- Form
- Tablet · Oral
- Labeler
- Acella Pharmaceuticals, LLC
- Type
- Human Prescription Drug
- Product code
- 42192-0327
Recalls naming this package
Class I · High risk
NP Thyroid 15
Subpotent Drug: FDA analysis found these products to be less than the labeled claim for the levothyroxine (T4) portion of the product.
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
- 42192-0329 NP Thyroid 30 3
- 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
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