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DICYCLOMINE HYDROCHLORIDE

NDC 73473-902, DICYCLOMINE HYDROCHLORIDE, tablet, from Solaris Pharma Corporation.

Product NDC
73473-902
Status
Listed
Labeler
Solaris Pharma Corporation
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216760
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/73473-902 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DICYCLOMINE HYDROCHLORIDE20 mg/1

Pharmacologic classes

Anticholinergic [EPC]; Cholinergic Antagonists [MoA]

Package NDCNDC-11Package
73473-902-0173473090201100 TABLET in 1 BOTTLE (73473-902-01)
73473-902-10734730902101000 TABLET in 1 BOTTLE (73473-902-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d46259e6-5eca-4356-bc18-815104c925cc

  • NADAC price for package 73473090201

    GET /v1/drugs/nadac/73473090201

  • NADAC price for package 73473090210

    GET /v1/drugs/nadac/73473090210

Use it

Look up 73473-902 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/73473-902 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 73473-902. 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.