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Dicyclomine hydrochloride

NDC 73352-119, Dicyclomine hydrochloride, tablet, from Trifluent Pharma, LLC.

Product NDC
73352-119
Status
Listed
Labeler
Trifluent Pharma, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216736
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/73352-119 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DICYCLOMINE HYDROCHLORIDE40 mg/1

Pharmacologic classes

Anticholinergic [EPC]; Cholinergic Antagonists [MoA]

Package NDCNDC-11Package
73352-119-607335201196060 TABLET in 1 BOTTLE (73352-119-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/56282794-5874-4220-b25c-cea4b17d19aa

Use it

Look up 73352-119 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/73352-119 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 73352-119. 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.