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Paroxetine

NDC 46708-767, Paroxetine, tablet, film coated, extended release, from Alembic Pharmaceuticals Limited.

Product NDC
46708-767
Status
Listed
Labeler
Alembic Pharmaceuticals Limited
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/46708-767 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PAROXETINE HYDROCHLORIDE HEMIHYDRATE25 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
46708-767-304670807673030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-767-30)
46708-767-91467080767911000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46708-767-91)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/59cb7de6-483d-4007-b6ef-f10a70b872e9

Use it

Look up 46708-767 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/46708-767 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 46708-767. 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.