DESIPRAMINE HYDROCHLORIDE
NDC 70518-4645, desipramine hydrochloride, tablet, from REMEDYREPACK INC..
- Product NDC
- 70518-4645
- Status
- Listed
- Labeler
- REMEDYREPACK INC.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA204963
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4645 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DESIPRAMINE HYDROCHLORIDE10 mg/1
Pharmacologic classes
Tricyclic Antidepressant [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70518-4645-0 | 70518464500 | 50 POUCH in 1 BOX (70518-4645-0) / 1 TABLET in 1 POUCH (70518-4645-1) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/dc1601be-e16a-411f-b9b8-01c51abb2441
Use it
Look up 70518-4645 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70518-4645 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70518-4645. 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.