Tapentadol Hydrochloride
NDC 72205-370, Tapentadol Hydrochloride, tablet, film coated, from Novadoz Pharmaceuticals LLC.
- Product NDC
- 72205-370
- Status
- Listed
- Labeler
- Novadoz Pharmaceuticals LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA220865
- DEA schedule
- CII
curl https://api.healthcare.dev/v1/drugs/ndc/72205-370 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- TAPENTADOL HYDROCHLORIDE75 mg/1
Pharmacologic classes
Opioid Agonist [EPC]; Opioid Agonists [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 72205-370-91 | 72205037091 | 100 TABLET, FILM COATED in 1 BOTTLE (72205-370-91) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/d4c5938a-68f0-46d2-9bad-8988d5724b09
Use it
Look up 72205-370 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72205-370 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72205-370. 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.