Glycerol Phenylbutyrate
NDC 0121-1049, Glycerol Phenylbutyrate, liquid, from PAI Holdings, LLC dba PAI Pharma.
- Product NDC
- 0121-1049
- Status
- Listed
- Labeler
- PAI Holdings, LLC dba PAI Pharma
- Dosage form
- LIQUID
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA220579
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0121-1049 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- GLYCEROL PHENYLBUTYRATE1.1 g/mL
Pharmacologic classes
Ammonium Ion Binding Activity [MoA]; Nitrogen Binding Agent [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0121-1049-25 | 00121104925 | 1 BOTTLE in 1 CARTON (0121-1049-25) / 25 mL in 1 BOTTLE |
Linked data
RxNorm, label and prices
RxNorm concepts
RxNorm links no concept to this product's packages.
Related lookups
FDA label sections
GET /v1/drugs/labels/35855917-12cb-4c18-b7c5-5f275c1c80f0
Use it
Look up 0121-1049 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0121-1049 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0121-1049. 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.