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Divalproex Sodium

NDC 65162-757, Divalproex Sodium, tablet, extended release, from Amneal Pharmaceuticals LLC.

Product NDC
65162-757
Status
Listed
Labeler
Amneal Pharmaceuticals LLC
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203730
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65162-757 \
  -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
65162-757-1065162075710100 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-757-10)
65162-757-5065162075750500 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-757-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7d3352ee-a240-43ff-a243-29ad2bc989c7

  • NADAC price for package 65162075710

    GET /v1/drugs/nadac/65162075710

  • NADAC price for package 65162075750

    GET /v1/drugs/nadac/65162075750

Use it

Look up 65162-757 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65162-757 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65162-757. 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.