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Dexmethylphenidate Hydrochloride

NDC 27808-091, dexmethylphenidate hydrochloride, tablet, from Cranbury Pharmaceuticals, LLC.

Product NDC
27808-091
Status
Listed
Labeler
Cranbury Pharmaceuticals, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207901
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/27808-091 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DEXMETHYLPHENIDATE HYDROCHLORIDE2.5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
27808-091-0127808009101100 TABLET in 1 BOTTLE, PLASTIC (27808-091-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1f2aa66a-51dc-459c-a765-5364bccd310f

  • NADAC price for package 27808009101

    GET /v1/drugs/nadac/27808009101

Use it

Look up 27808-091 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/27808-091 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 27808-091. 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.