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SERTRALINE HYDROCHLORIDE

NDC 42708-092, SERTRALINE HYDROCHLORIDE, tablet, film coated, from QPharma, Inc..

Product NDC
42708-092
Status
Listed
Labeler
QPharma, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202825
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42708-092 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SERTRALINE HYDROCHLORIDE50 mg/1

Pharmacologic classes

Cytochrome P450 2D6 Inhibitors [MoA]; Serotonin Reuptake Inhibitor [EPC]; Serotonin Uptake Inhibitors [MoA]

Package NDCNDC-11Package
42708-092-304270800923030 TABLET, FILM COATED in 1 BOTTLE (42708-092-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dc97a895-8c2f-4891-85f3-7f45e2396140

Use it

Look up 42708-092 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42708-092 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42708-092. 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.