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: a) M327D20-1, M327D20-3 Exp. 03/31/2022, M327H19-3A Exp. 07/31/2021, M327L19-1 Exp. 04/30/2021; b) M327D20-1 Exp. 03/31/2022 - Sep 17, 2020 · Class I · Acella Pharmaceuticals, LLC
Subpotent Drug: FDA analysis found these products to be less than the labeled claim for the levothyroxine (T4) portion of the product.
Lots: Lot #: M327E19-1 Exp. 10/2020
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
- 9.5 ug / 2.25 ug
- Approval
- unapproved drug other
- On the market since
- Nov 16, 2016
- Package NDCs
42192-327-0142192-327-3042192-327-90- Official label
- DailyMed (National Library of Medicine), updated Oct 13, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?