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Divalproex Sodium

NDC 0378-0472, divalproex sodium, tablet, film coated, extended release, from Mylan Pharmaceuticals Inc..

Product NDC
0378-0472
Status
Listed
Labeler
Mylan Pharmaceuticals Inc.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077567
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0378-0472 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DIVALPROEX SODIUM250 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
0378-0472-0100378047201100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-0472-01)
0378-0472-0500378047205500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-0472-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/00332c65-edad-a153-9c78-628931daa732
  • NADAC price for package 00378047201

    GET /v1/drugs/nadac/00378047201
  • NADAC price for package 00378047205

    GET /v1/drugs/nadac/00378047205

Use it

Look up 0378-0472 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0378-0472 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0378-0472. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.