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DICYCLOMINE HYDROCHLORIDE

NDC 73473-800, DICYCLOMINE HYDROCHLORIDE, capsule, from Solaris Pharma Corporation.

Product NDC
73473-800
Status
Listed
Labeler
Solaris Pharma Corporation
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216639
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/73473-800 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DICYCLOMINE HYDROCHLORIDE10 mg/1

Pharmacologic classes

Anticholinergic [EPC]; Cholinergic Antagonists [MoA]

Package NDCNDC-11Package
73473-800-0173473080001100 CAPSULE in 1 BOTTLE (73473-800-01)
73473-800-10734730800101000 CAPSULE in 1 BOTTLE (73473-800-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4237bb2e-d6dd-4e3a-baa2-85be5dc3c8f2

  • NADAC price for package 73473080001

    GET /v1/drugs/nadac/73473080001

  • NADAC price for package 73473080010

    GET /v1/drugs/nadac/73473080010

Use it

Look up 73473-800 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/73473-800 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 73473-800. 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.