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ATROPINE SULFATE

NDC 51662-1311, ATROPINE SULFATE, injection, from HF Acquisition Co LLC, DBA HealthFirst.

Product NDC
51662-1311
Status
Listed
Labeler
HF Acquisition Co LLC, DBA HealthFirst
Dosage form
INJECTION
Route
INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
UNAPPROVED DRUG OTHER
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51662-1311 \
  -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
51662-1311-15166213110120 mL in 1 VIAL, MULTI-DOSE (51662-1311-1)
51662-1311-35166213110325 POUCH in 1 CASE (51662-1311-3) / 1 mL in 1 POUCH (51662-1311-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/77935b57-fcf6-c88a-e053-2a91aa0a0a80

Use it

Look up 51662-1311 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51662-1311 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51662-1311. 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.