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Divalproex sodium

NDC 50090-6074, Divalproex sodium, tablet, film coated, extended release, from A-S Medication Solutions.

Product NDC
50090-6074
Status
Listed
Labeler
A-S Medication Solutions
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202419
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50090-6074 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DIVALPROEX SODIUM500 mg/1

Pharmacologic classes

Anti-epileptic Agent [EPC]; Decreased Central Nervous System Disorganized Electrical Activity [PE]; Mood Stabilizer [EPC]

Package NDCNDC-11Package
50090-6074-05009060740030 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6074-0)
50090-6074-15009060740190 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6074-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3df910c5-b6f0-4a65-9640-b702ecea49f9

Use it

Look up 50090-6074 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50090-6074 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50090-6074. 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.