TRAMADOL HYDROCHLORIDE
NDC 68180-698, TRAMADOL HYDROCHLORIDE, tablet, extended release, from Lupin Pharmaceuticals, Inc..
- Product NDC
- 68180-698
- Status
- Listed
- Labeler
- Lupin 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/68180-698 \ -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 |
|---|---|---|
| 68180-698-06 | 68180069806 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-698-06) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/46bb9ae6-3ee8-463c-badb-c7a45a89b84bNADAC price for package 68180069806
GET /v1/drugs/nadac/68180069806
Use it
Look up 68180-698 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68180-698 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68180-698. 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.