Duloxetine
NDC 25000-608, Duloxetine Hydrochloride, capsule, delayed release, from MARKSANS PHARMA LIMITED.
- Product NDC
- 25000-608
- Status
- Listed
- Labeler
- MARKSANS PHARMA LIMITED
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA090723
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/25000-608 \ -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 |
|---|---|---|
| 25000-608-06 | 25000060806 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (25000-608-06) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/3686cde5-f76d-4d16-aa5d-caceb8408f8c
Use it
Look up 25000-608 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/25000-608 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 25000-608. 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.