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Divalproex Sodium

NDC 37662-0731, Divalproex Sodium, pellet, from Hahnemann Laboratories, INC..

Product NDC
37662-0731
Status
Listed
Labeler
Hahnemann Laboratories, INC.
Dosage form
PELLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
UNAPPROVED HOMEOPATHIC
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/37662-0731 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VALPROATE SODIUM1 [hp_M]/1

Pharmacologic classes

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

Package NDCNDC-11Package
37662-0731-137662073101200 PELLET in 1 VIAL, GLASS (37662-0731-1)
37662-0731-237662073102500 PELLET in 1 VIAL, GLASS (37662-0731-2)
37662-0731-3376620731033000 PELLET in 1 BOTTLE, GLASS (37662-0731-3)
37662-0731-43766207310410000 PELLET in 1 BOTTLE, GLASS (37662-0731-4)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 37662-0731 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/37662-0731 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 37662-0731. 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.