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DICYCLOMINE HYDROCHLORIDE

NDC 70069-441, DICYCLOMINE HYDROCHLORIDE, injection, solution, from Somerset Therapeutics, LLC.

Product NDC
70069-441
Status
Listed
Labeler
Somerset Therapeutics, LLC
Dosage form
INJECTION, SOLUTION
Route
INTRAMUSCULAR
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214333
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70069-441 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DICYCLOMINE HYDROCHLORIDE10 mg/mL

Pharmacologic classes

Anticholinergic [EPC]; Cholinergic Antagonists [MoA]

Package NDCNDC-11Package
70069-441-05700690441055 AMPULE in 1 CARTON (70069-441-05) / 2 mL in 1 AMPULE (70069-441-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7ad77f59-e24a-406d-95bf-3d5c6cbc3cbe

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=70069-441

Use it

Look up 70069-441 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70069-441 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70069-441. 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.