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Atropine Sulfate

NDC 24208-825, Atropine Sulfate, ointment, from Bausch & Lomb Incorporated.

Product NDC
24208-825
Status
Listed
Labeler
Bausch & Lomb Incorporated
Dosage form
OINTMENT
Route
OPHTHALMIC
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
UNAPPROVED DRUG OTHER
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/24208-825 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ATROPINE SULFATE10 mg/g

Pharmacologic classes

Anticholinergic [EPC]; Cholinergic Antagonists [MoA]; Cholinergic Muscarinic Antagonist [EPC]; Cholinergic Muscarinic Antagonists [MoA]

Package NDCNDC-11Package
24208-825-55242080825551 TUBE in 1 CARTON (24208-825-55) / 3.5 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c0a56d60-0914-42b1-af59-c56afe93d18c

Use it

Look up 24208-825 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/24208-825 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 24208-825. 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.