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PAROXETINE

NDC 68180-645, PAROXETINE, tablet, film coated, extended release, from Lupin Pharmaceuticals, Inc..

Product NDC
68180-645
Status
Listed
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204134
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68180-645 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PAROXETINE HYDROCHLORIDE HEMIHYDRATE37.5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
68180-645-066818006450630 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68180-645-06)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d315e0da-f829-408b-be5d-2bca2e06913c

Use it

Look up 68180-645 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68180-645 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68180-645. 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.