Hydrochlorothiazide
NDC 42708-027, Hydrochlorothiazide, capsule, gelatin coated, from QPharma, Inc..
- Product NDC
- 42708-027
- Status
- Listed
- Labeler
- QPharma, Inc.
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA AUTHORIZED GENERIC
- Application
- NDA020504
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/42708-027 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- HYDROCHLOROTHIAZIDE12.5 mg/1
Pharmacologic classes
Increased Diuresis [PE]; Thiazide Diuretic [EPC]; Thiazides [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 42708-027-30 | 42708002730 | 30 CAPSULE, GELATIN COATED in 1 BOTTLE (42708-027-30) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/5bacc909-6b02-4815-85ef-55fd25b1b1f7
Use it
Look up 42708-027 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/42708-027 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 42708-027. 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.