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Carbidopa

NDC 68682-200, Carbidopa Tablets, tablet, from Oceanside Pharmaceuticals.

Product NDC
68682-200
Status
Listed
Labeler
Oceanside Pharmaceuticals
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA017830
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68682-200 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CARBIDOPA25 mg/1
Package NDCNDC-11Package
68682-200-2568682020025100 TABLET in 1 BOTTLE (68682-200-25)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d5204e5e-10ef-4758-8fc6-cb710048c687

Use it

Look up 68682-200 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68682-200 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68682-200. 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.