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Benzonatate

NDC 70518-4182, Benzonatate, capsule, from REMEDYREPACK INC..

Product NDC
70518-4182
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211518
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4182 \
  -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
70518-4182-07051841820030 CAPSULE in 1 BOTTLE, PLASTIC (70518-4182-0)
70518-4182-17051841820130 CAPSULE in 1 BLISTER PACK (70518-4182-1)
70518-4182-27051841820220 CAPSULE in 1 BOTTLE, PLASTIC (70518-4182-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9815f3f4-fb46-4796-a0ed-62a9e098286d

Use it

Look up 70518-4182 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4182 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4182. 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.