leuprolide acetate
NDC 47335-936, leuprolide acetate, kit, from Sun Pharmaceutical Industries, Inc..
- Product NDC
- 47335-936
- Status
- Listed
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- KIT
- Route
- —
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA078885
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/47335-936 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
None listed.
| Package NDC | NDC-11 | Package |
|---|---|---|
| 47335-936-40 | 47335093640 | 1 KIT in 1 CARTON (47335-936-40) * 1 VIAL, MULTI-DOSE in 1 CARTON / 2.8 mL in 1 VIAL, MULTI-DOSE * 1 mL in 1 PACKET |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/a3b01473-30c7-4945-bd60-2484221aaaadNADAC price for package 47335093640
GET /v1/drugs/nadac/47335093640
Use it
Look up 47335-936 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/47335-936 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 47335-936. 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.