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Tolcapone

NDC 68682-938, Tolcapone, tablet, film coated, from Oceanside Pharmaceuticals.

Product NDC
68682-938
Status
Listed
Labeler
Oceanside Pharmaceuticals
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA020697
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68682-938 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TOLCAPONE100 mg/1

Pharmacologic classes

Catechol O-Methyltransferase Inhibitors [MoA]; Catechol-O-Methyltransferase Inhibitor [EPC]

Package NDCNDC-11Package
68682-938-906868209389090 TABLET, FILM COATED in 1 BOTTLE (68682-938-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dd367eec-359a-4065-b5c3-7c0107c823fe

Use it

Look up 68682-938 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68682-938 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68682-938. 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.