HydrALAZINE Hydrochloride
NDC 71205-072, HydrALAZINE Hydrochloride, tablet, from Proficient Rx LP.
- Product NDC
- 71205-072
- Status
- Listed
- Labeler
- Proficient Rx LP
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA200770
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71205-072 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- HYDRALAZINE HYDROCHLORIDE50 mg/1
Pharmacologic classes
Arteriolar Vasodilation [PE]; Arteriolar Vasodilator [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71205-072-30 | 71205007230 | 30 TABLET in 1 BOTTLE (71205-072-30) |
| 71205-072-60 | 71205007260 | 60 TABLET in 1 BOTTLE (71205-072-60) |
| 71205-072-90 | 71205007290 | 90 TABLET in 1 BOTTLE (71205-072-90) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/dfd60a79-2a30-41e6-b000-a144730099a8
Use it
Look up 71205-072 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71205-072 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71205-072. 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.