Quinapril and Hydrochlorothiazide
NDC 62135-669, Quinapril and Hydrochlorothiazide, tablet, from Chartwell RX, LLC.
- Product NDC
- 62135-669
- Status
- Listed
- Labeler
- Chartwell RX, LLC
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA076374
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/62135-669 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- QUINAPRIL HYDROCHLORIDE20 mg/1
- HYDROCHLOROTHIAZIDE25 mg/1
Pharmacologic classes
Angiotensin Converting Enzyme Inhibitor [EPC]; Angiotensin-converting Enzyme Inhibitors [MoA]; Increased Diuresis [PE]; Thiazide Diuretic [EPC]; Thiazides [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 62135-669-90 | 62135066990 | 90 TABLET in 1 BOTTLE (62135-669-90) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/2eae533f-d0af-47e8-a1f2-94bc8cc89b5a
Use it
Look up 62135-669 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/62135-669 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 62135-669. 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.