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Atropine Sulfate

NDC 70069-716, Atropine Sulfate Monohydrate, solution/ drops, from Somerset Therapeutics, LLC.

Product NDC
70069-716
Status
Listed
Labeler
Somerset Therapeutics, LLC
Dosage form
SOLUTION/ DROPS
Route
OPHTHALMIC
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217791
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70069-716 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ATROPINE SULFATE10 mg/mL

Pharmacologic classes

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

Package NDCNDC-11Package
70069-716-01700690716011 BOTTLE in 1 CARTON (70069-716-01) / 5 mL in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/bfdb85b2-86d0-4f32-a8fa-272af48a191c

  • NADAC price for package 70069071601

    GET /v1/drugs/nadac/70069071601

Use it

Look up 70069-716 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70069-716 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70069-716. 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.