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Dexmethylphenidate Hydrochloride Extended-Release

NDC 0781-2732, dexmethylphenidate hydrochloride, capsule, extended release, from Sandoz Inc.

Product NDC
0781-2732
Status
Listed
Labeler
Sandoz Inc
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA021802
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0781-2732 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DEXMETHYLPHENIDATE HYDROCHLORIDE30 mg/1

Pharmacologic classes

Central Nervous System Stimulant [EPC]; Central Nervous System Stimulation [PE]

Package NDCNDC-11Package
0781-2732-310078127323130 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0781-2732-31)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/71f56227-d87a-4bc0-a879-c1993c6ccba6

Use it

Look up 0781-2732 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0781-2732 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0781-2732. 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.