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Benzonatate 200 mg

NDC 25000-003, Benzonatate 200 mg, capsule, liquid filled, from MARKSANS PHARMA LIMITED.

Product NDC
25000-003
Status
Listed
Labeler
MARKSANS PHARMA LIMITED
Dosage form
CAPSULE, LIQUID FILLED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA220298
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/25000-003 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BENZONATATE200 mg/1

Pharmacologic classes

Decreased Tracheobronchial Stretch Receptor Activity [PE]; Non-narcotic Antitussive [EPC]

Package NDCNDC-11Package
25000-003-032500000030330 CAPSULE, LIQUID FILLED in 1 BOTTLE (25000-003-03)
25000-003-0825000000308100 CAPSULE, LIQUID FILLED in 1 BOTTLE (25000-003-08)
25000-003-1225000000312500 CAPSULE, LIQUID FILLED in 1 BOTTLE (25000-003-12)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/44104cfc-df60-4d48-9fe1-53456a5e1974

Use it

Look up 25000-003 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/25000-003 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 25000-003. 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.