Drug
Who makes methylergonovine maleate?
12 companies list methylergonovine maleate as a human prescription drug, including under the names Methergine. Forms: injection; injection, solution; tablet. Routes: intramuscular, intravenous, oral.
Labellers from the openFDA NDC Directory. A labeller is the firm named on the label, not necessarily the site that made the product, and a listing is not an FDA approval. Data as of 24 Sept 2026. Methodology
Companies listing methylergonovine maleate
| Company | Forms | Application | NDCs | Registered sites |
|---|---|---|---|---|
| Bryant Ranch PrepackUnited States | injection | ANDAANDA040889 | 2 | 1 |
| HF Acquisition Co LLCUnited States | injection; injection, solution | ANDAANDA040889, ANDA090193 | 2 | 1 |
| Lupin LimitedIndia | tablet | ANDAANDA091577 | 1 | 14 |
| Granules Pharmaceuticals Inc.India | tablet | ANDAANDA210424 | 1 | 8 |
| Teva Pharmaceutical Industries Ltd.Canada | tablet | ANDAANDA211455 | 1 | 6 |
| American Regent, Inc.United States | injection, solution | ANDAANDA090193 | 1 | 5 |
| Pharma Packaging Solutions, LLC dba Tjoapack, LLCUnited States | tablet | ANDAANDA210424 | 1 | 5 |
| Rising Pharma Holdings, Inc.United States | tablet | ANDAANDA211919 | 1 | 1 |
| Breckenridge Pharmaceutical, Inc. | injection | ANDAANDA040889 | 1 | 0 |
| MAJOR Pharmaceuticals Inc. | tablet | ANDAANDA210424 | 1 | 0 |
| Pharmacist Pharmaceutical, LLC | injection, solution | ANDAANDA040889 | 1 | 0 |
| Volley Pharmaceuticals, LLC | tablet | ANDAANDA212233 | 1 | 0 |
Enquiry
Common questions
- Who makes methylergonovine maleate?
- 12 companies list methylergonovine maleate as a human prescription drug in the openFDA NDC Directory, led by Bryant Ranch Prepack, HF Acquisition Co LLC, Lupin Limited, Granules Pharmaceuticals Inc., Teva Pharmaceutical Industries Ltd.. Each is the labeller, the firm named on the label; the product may be made at a site registered to another company.
- Is there a generic methylergonovine maleate?
- 12 companies list methylergonovine maleate under an abbreviated new drug application (ANDA), the application type used for generics. Listing status is from the NDC Directory; it is not a statement of availability.