Buprenorphine and Naloxone Sublingual Film
NDC 47781-356, Buprenorphine and Naloxone, film, from Alvogen Inc..
- Product NDC
- 47781-356
- Status
- Listed
- Labeler
- Alvogen Inc.
- Dosage form
- FILM
- Route
- BUCCAL, SUBLINGUAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA205954
- DEA schedule
- CIII
curl https://api.healthcare.dev/v1/drugs/ndc/47781-356 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- BUPRENORPHINE HYDROCHLORIDE4 mg/1
- NALOXONE HYDROCHLORIDE DIHYDRATE1 mg/1
Pharmacologic classes
Opioid Antagonist [EPC]; Opioid Antagonists [MoA]; Partial Opioid Agonist [EPC]; Partial Opioid Agonists [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 47781-356-03 | 47781035603 | 30 POUCH in 1 CARTON (47781-356-03) / 1 FILM in 1 POUCH (47781-356-11) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/4210afeb-474c-d842-d68e-af7e0021851aNADAC price for package 47781035603
GET /v1/drugs/nadac/47781035603
Use it
Look up 47781-356 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/47781-356 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 47781-356. 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.