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VALPROIC ACID

NDC 70518-3805, VALPROIC ACID, solution, from REMEDYREPACK INC..

Product NDC
70518-3805
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075379
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3805 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VALPROIC ACID250 mg/5mL

Pharmacologic classes

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

Package NDCNDC-11Package
70518-3805-07051838050010 CUP, UNIT-DOSE in 1 BOX (70518-3805-0) / 5 mL in 1 CUP, UNIT-DOSE (70518-3805-1)
70518-3805-27051838050210 CUP, UNIT-DOSE in 1 BOX (70518-3805-2) / 10 mL in 1 CUP, UNIT-DOSE (70518-3805-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/65c1589e-c591-4b79-b75e-884c0d609ae8

Use it

Look up 70518-3805 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3805 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3805. 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.