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Trihexyphenidyl Hydrochloride

NDC 63850-0022, Trihexyphenidyl Hydrochloride, tablet, from Natco Pharma Limited.

Product NDC
63850-0022
Status
Listed
Labeler
Natco Pharma Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA091630
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63850-0022 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TRIHEXYPHENIDYL HYDROCHLORIDE5 mg/1
Package NDCNDC-11Package
63850-0022-163850002201100 TABLET in 1 BOTTLE (63850-0022-1)
63850-0022-2638500022021000 TABLET in 1 BOTTLE (63850-0022-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b7e4200c-feff-4537-aad1-cf9989fd8c14

Use it

Look up 63850-0022 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63850-0022 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63850-0022. 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.