VALPROIC ACID
NDC 0121-0675, VALPROIC ACID, solution, from PAI Holdings, LLC dba PAI Pharma.
- Product NDC
- 0121-0675
- Status
- Listed
- Labeler
- PAI Holdings, LLC dba PAI Pharma
- Dosage form
- SOLUTION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA075379
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0121-0675 \ -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 NDC | NDC-11 | Package |
|---|---|---|
| 0121-0675-85 | 00121067585 | 473 mL in 1 BOTTLE (0121-0675-85) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/7d5cb52e-37dd-4dfa-a6f4-09f9548846c6NADAC price for package 00121067585
GET /v1/drugs/nadac/00121067585
Use it
Look up 0121-0675 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0121-0675 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0121-0675. 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.