TRAMADOL HYDROCHLORIDE
NDC 61919-893, TRAMADOL HYDROCHLORIDE, tablet, extended release, from DIRECT RX.
- Product NDC
- 61919-893
- Status
- Listed
- Labeler
- DIRECT RX
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA201384
- DEA schedule
- CIV
curl https://api.healthcare.dev/v1/drugs/ndc/61919-893 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- TRAMADOL HYDROCHLORIDE200 mg/1
Pharmacologic classes
Full Opioid Agonists [MoA]; Opioid Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 61919-893-30 | 61919089330 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-893-30) |
| 61919-893-60 | 61919089360 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-893-60) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/5285f056-c32c-4e7a-bec6-3a726aa23d5a
Use it
Look up 61919-893 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/61919-893 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 61919-893. 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.