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Benzonatate

NDC 70518-2491, Benzonatate, capsule, from REMEDYREPACK INC..

Product NDC
70518-2491
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206948
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2491 \
  -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
70518-2491-37051824910330 CAPSULE in 1 BOTTLE, PLASTIC (70518-2491-3)
70518-2491-47051824910421 CAPSULE in 1 BOTTLE, PLASTIC (70518-2491-4)
70518-2491-57051824910520 CAPSULE in 1 BOTTLE, PLASTIC (70518-2491-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ed756746-4cbb-4196-a972-5a8c23702b2a

Use it

Look up 70518-2491 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2491 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-2491. 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.