Amitriptyline Hydrochloride
NDC 70771-1173, Amitriptyline Hydrochloride, tablet, film coated, from Zydus Lifesciences Limited.
- Product NDC
- 70771-1173
- Status
- Listed
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA210086
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1173 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- AMITRIPTYLINE HYDROCHLORIDE10 mg/1
Pharmacologic classes
Tricyclic Antidepressant [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70771-1173-0 | 70771117300 | 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1173-0) |
| 70771-1173-1 | 70771117301 | 100 TABLET, FILM COATED in 1 BOTTLE (70771-1173-1) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/4159b10e-f589-486c-969d-9b4544b098b5
Use it
Look up 70771-1173 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1173 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70771-1173. 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.