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Atropine Sulfate

NDC 70518-3120, Atropine Sulfate, injection, from REMEDYREPACK INC..

Product NDC
70518-3120
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
INJECTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212461
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3120 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ATROPINE SULFATE.1 mg/mL

Pharmacologic classes

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

Package NDCNDC-11Package
70518-3120-07051831200010 CARTON in 1 PACKAGE (70518-3120-0) / 1 SYRINGE in 1 CARTON / 10 mL in 1 SYRINGE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/46ba6000-b842-449a-8dd4-7bb9dc7a74c5

Use it

Look up 70518-3120 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3120 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3120. 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.