Drug
Who makes tramadol hydrochloride and acetaminophen?
11 companies list tramadol hydrochloride and acetaminophen as a human prescription drug. Forms: tablet; tablet, film coated. Routes: 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 tramadol hydrochloride and acetaminophen
| Company | Forms | Application | NDCs | Registered sites |
|---|---|---|---|---|
| Bryant Ranch PrepackUnited States | tablet; tablet, film coated | ANDAANDA090485, ANDA207152 | 3 | 1 |
| ASCLEMED USA INC. DBA ENOVACHEMUnited States | tablet; tablet, film coated | ANDAANDA090485, ANDA201952 | 2 | 1 |
| Proficient Rx LPUnited States | tablet; tablet, film coated | ANDAANDA090485, ANDA207152 | 2 | 1 |
| Amneal Pharmaceuticals of New York, LLCIndia | tablet | ANDAANDA090485 | 1 | 14 |
| Aurobindo Pharma LimitedIndia | tablet, film coated | ANDAANDA207152 | 1 | 6 |
| Direct RxUnited States | tablet, film coated | ANDAANDA207152 | 1 | 1 |
| MedSource LabsUnited States | tablet, film coated | ANDAANDA207152 | 1 | 1 |
| Preferred Pharmaceuticals Inc.United States | tablet | ANDAANDA090485 | 1 | 1 |
| RemedyRepack, IncUnited States | tablet, film coated | ANDAANDA207152 | 1 | 1 |
| St. Mary's Medical Park PharmacyUnited States | tablet, film coated | ANDAANDA207152 | 1 | 1 |
| AvPAK | tablet | ANDAANDA090485 | 1 | 0 |
Enquiry
Common questions
- Who makes tramadol hydrochloride and acetaminophen?
- 11 companies list tramadol hydrochloride and acetaminophen as a human prescription drug in the openFDA NDC Directory, led by Bryant Ranch Prepack, ASCLEMED USA INC. DBA ENOVACHEM, Proficient Rx LP, Amneal Pharmaceuticals of New York, LLC, Aurobindo Pharma 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 tramadol hydrochloride and acetaminophen?
- 11 companies list tramadol hydrochloride and acetaminophen 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.