Desipramine Hydrochloride
NDC 69238-1063, Desipramine, tablet, film coated, from Amneal Pharmaceuticals LLC.
- Product NDC
- 69238-1063
- Status
- Listed
- Labeler
- Amneal Pharmaceuticals LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA208105
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/69238-1063 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DESIPRAMINE HYDROCHLORIDE150 mg/1
Pharmacologic classes
Tricyclic Antidepressant [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 69238-1063-2 | 69238106302 | 50 TABLET, FILM COATED in 1 BOTTLE (69238-1063-2) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/a3b4b25d-0ddb-4531-badb-f1ba3168ac07NADAC price for package 69238106302
GET /v1/drugs/nadac/69238106302
Use it
Look up 69238-1063 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/69238-1063 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 69238-1063. 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.