AMITRIPTYLINE HYDROCHLORIDE
NDC 59651-819, AMITRIPTYLINE HYDROCHLORIDE, tablet, film coated, from Aurobindo Pharma Limited.
- Product NDC
- 59651-819
- Status
- Listed
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA086009
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/59651-819 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- AMITRIPTYLINE HYDROCHLORIDE50 mg/1
Pharmacologic classes
Tricyclic Antidepressant [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 59651-819-01 | 59651081901 | 100 TABLET, FILM COATED in 1 BOTTLE (59651-819-01) |
| 59651-819-99 | 59651081999 | 1000 TABLET, FILM COATED in 1 BOTTLE (59651-819-99) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/8085a37f-3c76-4f74-aab3-9a929a7eb1c2
Use it
Look up 59651-819 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/59651-819 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 59651-819. 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.