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TRIHEXYPHENIDYL HYDROCHLORIDE

NDC 70954-212, TRIHEXYPHENIDYL HYDROCHLORIDE, tablet, from Novitium Pharma LLC.

Product NDC
70954-212
Status
Listed
Labeler
Novitium Pharma LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040254
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70954-212 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TRIHEXYPHENIDYL HYDROCHLORIDE2 mg/1
Package NDCNDC-11Package
70954-212-1070954021210100 TABLET in 1 BOTTLE (70954-212-10)
70954-212-20709540212201000 TABLET in 1 BOTTLE (70954-212-20)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/83608c13-509d-448b-8559-5f5e8a9a0d75
  • NADAC price for package 70954021210

    GET /v1/drugs/nadac/70954021210
  • NADAC price for package 70954021220

    GET /v1/drugs/nadac/70954021220

Use it

Look up 70954-212 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70954-212 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70954-212. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.