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SERTRALINE HYDROCHLORIDE

NDC 71205-028, SERTRALINE HYDROCHLORIDE, tablet, film coated, from Proficient Rx LP.

Product NDC
71205-028
Status
Listed
Labeler
Proficient Rx LP
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/71205-028 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SERTRALINE HYDROCHLORIDE50 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
71205-028-307120500283030 TABLET, FILM COATED in 1 BOTTLE (71205-028-30)
71205-028-607120500286060 TABLET, FILM COATED in 1 BOTTLE (71205-028-60)
71205-028-907120500289090 TABLET, FILM COATED in 1 BOTTLE (71205-028-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6b532e6a-b040-4a10-a242-fb6d8dfc0852

Use it

Look up 71205-028 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-028 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-028. 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.