Duloxetine
NDC 76420-623, Duloxetine, capsule, delayed release, from Asclemed USA, Inc..
- Product NDC
- 76420-623
- Status
- Listed
- Labeler
- Asclemed USA, Inc.
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA208706
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/76420-623 \ -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 |
|---|---|---|
| 76420-623-00 | 76420062300 | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-623-00) |
| 76420-623-01 | 76420062301 | 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-623-01) |
| 76420-623-20 | 76420062320 | 20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-623-20) |
| 76420-623-30 | 76420062330 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-623-30) |
| 76420-623-60 | 76420062360 | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-623-60) |
| 76420-623-90 | 76420062390 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (76420-623-90) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/f61bd9f3-cd3d-4c76-a110-0f1dcba610af
Use it
Look up 76420-623 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/76420-623 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 76420-623. 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.