Duloxetine
NDC 42708-196, Duloxetine, capsule, delayed release, from QPharma, Inc..
- Product NDC
- 42708-196
- Status
- Listed
- Labeler
- QPharma, Inc.
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA090694
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/42708-196 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DULOXETINE HYDROCHLORIDE60 mg/1
Pharmacologic classes
Norepinephrine Uptake Inhibitors [MoA]; Serotonin Uptake Inhibitors [MoA]; Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 42708-196-30 | 42708019630 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (42708-196-30) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/4f205401-39ac-7009-e063-6394a90aaa8c
Use it
Look up 42708-196 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/42708-196 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 42708-196. 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.