Tramadol Hydrochloride
NDC 82804-298, Tramadol Hydrochloride, tablet, film coated, extended release, from Proficient Rx LP.
- Product NDC
- 82804-298
- Status
- Listed
- Labeler
- Proficient Rx LP
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA209404
- DEA schedule
- CIV
curl https://api.healthcare.dev/v1/drugs/ndc/82804-298 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- TRAMADOL HYDROCHLORIDE100 mg/1
Pharmacologic classes
Full Opioid Agonists [MoA]; Opioid Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 82804-298-30 | 82804029830 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (82804-298-30) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/aefc85bc-0820-4aee-8d94-313c5f1658f5
Use it
Look up 82804-298 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/82804-298 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 82804-298. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.