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duloxetine

NDC 70954-861, duloxetine, capsule, delayed release, from ANI Pharmaceuticals, Inc..

Product NDC
70954-861
Status
Listed
Labeler
ANI Pharmaceuticals, Inc.
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202336
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70954-861 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DULOXETINE HYDROCHLORIDE30 mg/1

Pharmacologic classes

Norepinephrine Uptake Inhibitors [MoA]; Serotonin Uptake Inhibitors [MoA]; Serotonin and Norepinephrine Reuptake Inhibitor [EPC]

Package NDCNDC-11Package
70954-861-207095408612090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70954-861-20)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fb37745f-fb40-4f7f-8143-ea1874c38e1b

Use it

Look up 70954-861 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70954-861 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70954-861. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.