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Paroxetine

NDC 70518-3518, Paroxetine, tablet, film coated, from REMEDYREPACK INC..

Product NDC
70518-3518
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077584
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3518 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PAROXETINE HYDROCHLORIDE HEMIHYDRATE20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
70518-3518-070518351800100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3518-0)
70518-3518-17051835180130 TABLET, FILM COATED in 1 BLISTER PACK (70518-3518-1)
70518-3518-270518351802100 POUCH in 1 BOX (70518-3518-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-3518-3)
70518-3518-47051835180430 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3518-4)
70518-3518-67051835180645 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3518-6)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/05ec70fd-4c65-495f-ba12-e8433a10b655

Use it

Look up 70518-3518 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3518 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3518. 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.