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Atropine Sulfate

NDC 70069-641, Atropine Sulfate, solution, from Somerset Therapeutics, LLC.

Product NDC
70069-641
Status
Listed
Labeler
Somerset Therapeutics, LLC
Dosage form
SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215969
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70069-641 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ATROPINE SULFATE1 mg/mL

Pharmacologic classes

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

Package NDCNDC-11Package
70069-641-257006906412525 VIAL in 1 CARTON (70069-641-25) / 1 mL in 1 VIAL (70069-641-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a6fac578-c7bc-4b3c-a454-7889cc819118

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=70069-641

Use it

Look up 70069-641 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70069-641 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70069-641. 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.