Duloxetine
NDC 71205-525, Duloxetine, capsule, delayed release pellets, from Proficient Rx LP.
- Product NDC
- 71205-525
- Status
- Listed
- Labeler
- Proficient Rx LP
- Dosage form
- CAPSULE, DELAYED RELEASE PELLETS
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA090776
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71205-525 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DULOXETINE HYDROCHLORIDE20 mg/1
Pharmacologic classes
Norepinephrine Uptake Inhibitors [MoA]; Serotonin Uptake Inhibitors [MoA]; Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71205-525-30 | 71205052530 | 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71205-525-30) |
| 71205-525-60 | 71205052560 | 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71205-525-60) |
| 71205-525-90 | 71205052590 | 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71205-525-90) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/3dec1805-9a95-462e-8784-303004d500b1
Use it
Look up 71205-525 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71205-525 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71205-525. 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.