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Paroxetine

NDC 62332-768, Paroxetine, tablet, film coated, extended release, from Alembic Pharmaceuticals Inc..

Product NDC
62332-768
Status
Listed
Labeler
Alembic Pharmaceuticals Inc.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217280
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62332-768 \
  -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
62332-768-306233207683030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62332-768-30)
62332-768-91623320768911000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62332-768-91)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5da839f9-e2bf-4b83-a410-1226ba4552a1

Use it

Look up 62332-768 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62332-768 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62332-768. 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.