Cyproheptadine Hydrochloride
NDC 76385-130, Cyproheptadine Hydrochloride, tablet, from UNICHEM PHARMACEUTICALS (USA), INC..
- Product NDC
- 76385-130
- Status
- Listed
- Labeler
- UNICHEM PHARMACEUTICALS (USA), INC.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA206676
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/76385-130 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- CYPROHEPTADINE HYDROCHLORIDE4 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 76385-130-01 | 76385013001 | 100 TABLET in 1 BOTTLE (76385-130-01) |
| 76385-130-10 | 76385013010 | 1000 TABLET in 1 BOTTLE (76385-130-10) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/99fb821a-fe33-4468-9026-9729a8deff08NADAC price for package 76385013001
GET /v1/drugs/nadac/76385013001
Use it
Look up 76385-130 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/76385-130 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 76385-130. 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.