Tramadol Hydrochloride
NDC 87441-089, Tramadol Hydrochloride, tablet, coated, from Unit Dose Solutions, Inc..
- Product NDC
- 87441-089
- Status
- Listed
- Labeler
- Unit Dose Solutions, Inc.
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA076003
- DEA schedule
- CIV
curl https://api.healthcare.dev/v1/drugs/ndc/87441-089 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- TRAMADOL HYDROCHLORIDE50 mg/1
Pharmacologic classes
Full Opioid Agonists [MoA]; Opioid Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 87441-089-01 | 87441008901 | 30 TABLET, COATED in 1 BLISTER PACK (87441-089-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/5c2ac7cb-3a38-2174-e063-6394a90a95cc
Use it
Look up 87441-089 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/87441-089 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 87441-089. 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.