sapropterin dihydrochloride
NDC 49884-720, sapropterin dihydrochloride, tablet, from Par Health USA, LLC.
- Product NDC
- 49884-720
- Status
- Listed
- Labeler
- Par Health USA, LLC
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA207200
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/49884-720 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SAPROPTERIN DIHYDROCHLORIDE100 mg/1
Pharmacologic classes
Breast Cancer Resistance Protein Inhibitors [MoA]; P-Glycoprotein Inhibitors [MoA]; Phenylalanine Hydroxylase Activator [EPC]; Phenylalanine Hydroxylase Activators [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 49884-720-08 | 49884072008 | 120 TABLET in 1 BOTTLE (49884-720-08) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/eafec3a2-4f29-4afa-8728-a62b34cefd18
Use it
Look up 49884-720 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/49884-720 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 49884-720. 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.