NDC 42192-331

NP Thyroid 90 57 ug / 13.5 ug tablet

On the label: Acella Pharmaceuticals, LLC.

Where it's 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 Acella Pharmaceuticals, LLC names for other drugs.

Recalls

Apr 29, 2021 · Class I · Acella Pharmaceuticals, LLC
Subpotent Drug
Lots: Lots: M331J19-10A, M331J19-11, M331J19-2A, M331J19-6A, Exp. 08/31/2021, M331K19-1, M331K19-2, M331K19-6, Exp. 09/30/2021
May 22, 2020 · Class I · Acella Pharmaceuticals, LLC
Superpotent Drug.
Lots: Lots: M331G18-1 Exp. JUN-2020, M331J18-1, M331J18-2, Exp. AUG-2020, M331M18-1, M331M18-2 Exp. NOV-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: Levothyroxine and Liothyronine: every company that makes it
Form: tablet, oral
Strength: 57 ug / 13.5 ug
Approval: unapproved drug other
On the market since: Feb 3, 2011
Package NDCs: 42192-331-01 42192-331-10 42192-331-30 42192-331-90
Official label: DailyMed (National Library of Medicine), updated Oct 13, 2026

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