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Sertraline Hydrochloride

NDC 70518-2812, Sertraline Hydrochloride, tablet, film coated, from REMEDYREPACK INC..

Product NDC
70518-2812
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077206
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2812 \
  -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
70518-2812-17051828120190 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2812-1)
70518-2812-27051828120230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2812-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/91e24d17-ff0a-449c-9472-b9df74c98456

Use it

Look up 70518-2812 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2812 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-2812. 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.