Duloxetine Delayed-Release
NDC 71610-736, DULOXETINE HYDROCHLORIDE, capsule, delayed release pellets, from Aphena Pharma Solutions - Tennessee, LLC.
- Product NDC
- 71610-736
- Status
- Listed
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Dosage form
- CAPSULE, DELAYED RELEASE PELLETS
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA203088
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71610-736 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DULOXETINE HYDROCHLORIDE30 mg/1
Pharmacologic classes
Norepinephrine Uptake Inhibitors [MoA]; Serotonin Uptake Inhibitors [MoA]; Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71610-736-42 | 71610073642 | 1800 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-736-42) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/dcfd62c7-1687-4e9b-9ae4-5a44929ac765
Use it
Look up 71610-736 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71610-736 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71610-736. 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.