Quick answers
- What is Methimazole used for?
- The FDA-approved label (Methimazole, Remedyrepack Inc., September 9, 2026) says: “Methimazole tablets are indicated: In patients with Graves' disease with hyperthyroidism or toxic multinodular goiter for whom surgery or radioactive iodine therapy is not an appropriate treatment option. To ameliorate symptoms of hyperthyroidism in preparation for thyroidectomy or radioactive iodine therapy.” This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
- Does Methimazole have a boxed warning?
- No. None of the 39 FDA labels we found for this medicine has a boxed warning.
- Is there a shortage of Methimazole?
- No current shortage is listed by the FDA for the products of this medicine (FDA data from October 30, 2026).
- Has Methimazole been recalled?
- No recall linked to the products of this medicine appears in the FDA enforcement reports we use.
- Who makes Methimazole?
- 21 companies list prescription products of Methimazole in the FDA NDC Directory, including Bryant Ranch Prepack, Preferred Pharmaceuticals Inc. and Remedyrepack Inc..
What Methimazole is used for
Quoted from the “Indications and Usage” section of the FDA-approved label.
Methimazole tablets are indicated: In patients with Graves' disease with hyperthyroidism or toxic multinodular goiter for whom surgery or radioactive iodine therapy is not an appropriate treatment option. To ameliorate symptoms of hyperthyroidism in preparation for thyroidectomy or radioactive iodine therapy.
— FDA label: Methimazole, Remedyrepack Inc., effective September 9, 2026. Read the full label on DailyMed →
The FDA has 39 labels for products of this medicine (different makers and forms); uses can differ between them. Check the label that comes with your own medicine.
This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
Boxed warning
A boxed warning (“black box”) is the FDA’s strongest warning on a drug label, for serious or life-threatening risks.
The label quoted above has no boxed warning.
0 of 39 FDA labels for this medicine have a boxed warning.
Forms and how it is given
| Dosage forms | Tablet |
|---|---|
| Route | Oral |
| Prescription products | 54 in the FDA NDC Directory |
What pharmacies pay (NADAC)
The National Average Drug Acquisition Cost (NADAC) is the average price U.S. retail pharmacies paid to buy one unit of a medicine (one tablet, one mL or one gram), from a monthly survey of pharmacy invoices by the Centers for Medicare & Medicaid Services (CMS). State Medicaid programs use it to pay pharmacies.
This is not the price you pay. What you pay depends on your insurance (copay or coinsurance), your pharmacy and any discounts, and pharmacies also charge for filling a prescription. Ask your pharmacist or your health plan what your price will be.
| Strength and form | Generic or brand | Pharmacies pay |
|---|---|---|
| methimazole 10 mg tablet | Generic | $0.1187 per tablet |
| methimazole 5 mg tablet | Generic | $0.0694 per tablet |
NADAC list of November 4, 2026; these prices took effect on October 21, 2026. Shown only where a package’s NDC code matches the NADAC list exactly, and only for that exact strength and form: nothing is averaged across strengths. Strengths and forms not listed here have no NADAC price.
Source: NADAC (National Average Drug Acquisition Cost) 2026, data.medicaid.gov (CMS) →
Companies that list this medicine
Labelers in the FDA NDC Directory: the company named on the package (maker or distributor), with the number of prescription products.
- Bryant Ranch Prepack13 products
- Preferred Pharmaceuticals Inc.4 products
- Remedyrepack Inc.3 products
- Viona Pharmaceuticals Inc2 products
- American Health Packaging2 products
- Rising Pharma Holdings, Inc.2 products
- Macleods Pharmaceuticals Limited2 products
- Golden State Medical Supply, Inc.2 products
- Coupler LLC2 products
- AvKARE2 products
- Upsher-Smith Laboratories, LLC2 products
- Bionpharma Inc.2 products
- Square Pharmaceuticals PLC.2 products
- AvPAK2 products
- Chartwell RX, LLC2 products
- NorthStar Rx LLC2 products
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.2 products
- Strides Pharma Science Limited2 products
- AiPing Pharmaceutical, Inc.2 products
- A-S Medication Solutions1 product
- Proficient Rx LP1 product
FDA approval history
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
Generic approvals (8)
- ANDA040350Mylan · March 29, 2000
- ANDA040411Chartwell Rx · March 27, 2001
- ANDA040547Aiping Pharm Inc · February 18, 2005
- ANDA040734Heritage Pharma · December 14, 2007
- ANDA202068Rising · March 7, 2012
- ANDA209827Macleods Pharms · May 24, 2023
- ANDA218149Bionpharma · September 25, 2023
- ANDA218830Square Pharms PLC · February 5, 2025
Shortage status
The FDA drug shortage list does not show these products.
Recalls
No recall linked to these products (by their NDC code) appears in the FDA enforcement reports.
Official identifiers
| RxCUI (RxNorm) | 197941, 197942 |
|---|---|
| SPL set ID of the quoted label | f69edfa9-0efb-4fe8-aeab-50f7baeebb6a |
| FDA labels (SPL) | 39 |
| FDA applications | 8 ANDA |
| Active ingredients (FDA) | METHIMAZOLE |
Sources
- FDA-approved label on DailyMed (National Library of Medicine) — Methimazole, Remedyrepack Inc., effective September 9, 2026; via openFDA, FDA data exported October 30, 2026, retrieved October 31, 2026
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- Drug shortages (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
openFDA data is provided by the FDA as is; it may be incomplete. Always rely on the label that comes with your medicine. FDA Enforcement Report search →