Entacapone
NDC 47335-007, Entacapone, tablet, film coated, from Sun Pharmaceutical Industries, Inc..
- Product NDC
- 47335-007
- Status
- Listed
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA AUTHORIZED GENERIC
- Application
- NDA020796
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/47335-007 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ENTACAPONE200 mg/1
Pharmacologic classes
Catechol O-Methyltransferase Inhibitors [MoA]; Catechol-O-Methyltransferase Inhibitor [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 47335-007-88 | 47335000788 | 100 TABLET, FILM COATED in 1 BOTTLE (47335-007-88) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/205522fb-bb0e-414e-a413-a08bef727653
Use it
Look up 47335-007 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/47335-007 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 47335-007. 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.