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ACAMPROSATE CALCIUM

NDC 70069-860, ACAMPROSATE CALCIUM, tablet, delayed release, from Somerset Therapeutics, LLC.

Product NDC
70069-860
Status
Listed
Labeler
Somerset Therapeutics, LLC
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218984
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70069-860 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ACAMPROSATE CALCIUM333 mg/1
Package NDCNDC-11Package
70069-860-1870069086018180 TABLET, DELAYED RELEASE in 1 BOTTLE (70069-860-18)
70069-860-307006908603030 TABLET, DELAYED RELEASE in 1 BOTTLE (70069-860-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1cfe4675-766f-4f1a-b1a8-96bbdacfcfa5

  • NADAC price for package 70069086018

    GET /v1/drugs/nadac/70069086018

Use it

Look up 70069-860 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70069-860 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70069-860. 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.