Tapentadol Hydrochloride
NDC 73190-081, Tapentadol Hydrochloride, tablet, film coated, from AvKARE.
- Product NDC
- 73190-081
- Status
- Listed
- Labeler
- AvKARE
- 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/73190-081 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- TAPENTADOL HYDROCHLORIDE50 mg/1
Pharmacologic classes
Opioid Agonist [EPC]; Opioid Agonists [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 73190-081-01 | 73190008101 | 100 TABLET, FILM COATED in 1 BOTTLE (73190-081-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/5b769a76-5ca5-b2e9-e063-6394a90a1b1b
Use it
Look up 73190-081 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/73190-081 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 73190-081. 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.