Drug
Who makes ndac and ee tablets and ferrous fumarate tablets?
2 companies list ndac and ee tablets and ferrous fumarate tablets as a human prescription drug, including under the names Tilia Fe. Forms: kit.
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 ndac and ee tablets and ferrous fumarate tablets
| Company | Forms | Application | NDCs | Registered sites |
|---|---|---|---|---|
| Mayne Pharma International Pty Ltd.Australia | kit | ANDAANDA202962 | 1 | 1 |
| Dr. Reddys Laboratories Limited | kit | ANDAANDA202962 | 1 | 0 |
Enquiry
Common questions
- Who makes ndac and ee tablets and ferrous fumarate tablets?
- 2 companies list ndac and ee tablets and ferrous fumarate tablets as a human prescription drug in the openFDA NDC Directory, led by Mayne Pharma International Pty Ltd., Dr. Reddys Laboratories Limited. 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 ndac and ee tablets and ferrous fumarate tablets?
- 2 companies list ndac and ee tablets and ferrous fumarate tablets 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.