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Atropine Sulfate

NDC 70518-4329, Atropine Sulfate, injection, from REMEDYREPACK INC..

Product NDC
70518-4329
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
INJECTION
Route
ENDOTRACHEAL, INTRAMEDULLARY, INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213561
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4329 \
  -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
70518-4329-07051843290010 VIAL in 1 CARTON (70518-4329-0) / 20 mL in 1 VIAL (70518-4329-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8663ff94-8bea-4061-9fd5-3ab2e85e862e

Use it

Look up 70518-4329 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4329 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-4329. 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.