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duloxetine

NDC 70247-012, Duloxetine, capsule, delayed release, from Qingdao BAHEAL Pharmaceutical Co., Ltd..

Product NDC
70247-012
Status
Listed
Labeler
Qingdao BAHEAL Pharmaceutical Co., Ltd.
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210599
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70247-012 \
  -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
70247-012-067024700120660 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70247-012-06)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e428429e-e1ea-40e1-870f-134533dc3aa1

Use it

Look up 70247-012 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70247-012 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70247-012. 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.