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Duloxetine

NDC 50090-7812, Duloxetine, capsule, delayed release, from A-S Medication Solutions.

Product NDC
50090-7812
Status
Listed
Labeler
A-S Medication Solutions
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208706
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50090-7812 \
  -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 NDCNDC-11Package
50090-7812-05009078120090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7812-0)
50090-7812-15009078120130 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7812-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7685a825-3c06-433d-ba98-4019c6ed2583

Use it

Look up 50090-7812 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50090-7812 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50090-7812. 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.