TRAMADOL HYDROCHLORIDE
NDC 68071-1671, TRAMADOL HYDROCHLORIDE, tablet, extended release, from NuCare Pharmaceuticals,Inc..
- Product NDC
- 68071-1671
- Status
- Listed
- Labeler
- NuCare Pharmaceuticals,Inc.
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA200503
- DEA schedule
- CIV
curl https://api.healthcare.dev/v1/drugs/ndc/68071-1671 \ -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 |
|---|---|---|
| 68071-1671-3 | 68071167103 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-1671-3) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/93c9c960-afbf-6d3d-e053-2995a90a8d15
Use it
Look up 68071-1671 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68071-1671 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68071-1671. 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.