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Atropine Sulfate

NDC 70069-481, Atropine Sulfate monohydrate, solution, from Somerset Therapeutics, LLC.

Product NDC
70069-481
Status
Listed
Labeler
Somerset Therapeutics, LLC
Dosage form
SOLUTION
Route
ENDOTRACHEAL, INTRAMEDULLARY, INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215005
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70069-481 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ATROPINE SULFATE.4 mg/mL

Pharmacologic classes

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

Package NDCNDC-11Package
70069-481-107006904811010 VIAL in 1 CARTON (70069-481-10) / 20 mL in 1 VIAL (70069-481-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/84ba1689-3030-48d5-9cce-70b5a24a4033

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=70069-481

Use it

Look up 70069-481 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70069-481 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70069-481. 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.