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Fosinopril Sodium and Hydrochlorothiazide

NDC 65862-309, Fosinopril Sodium and Hydrochlorothiazide, tablet, from Aurobindo Pharma Limited.

Product NDC
65862-309
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA079245
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65862-309 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FOSINOPRIL SODIUM20 mg/1
  • HYDROCHLOROTHIAZIDE12.5 mg/1

Pharmacologic classes

Angiotensin Converting Enzyme Inhibitor [EPC]; Angiotensin-converting Enzyme Inhibitors [MoA]; Increased Diuresis [PE]; Thiazide Diuretic [EPC]; Thiazides [CS]

Package NDCNDC-11Package
65862-309-0165862030901100 TABLET in 1 BOTTLE (65862-309-01)
65862-309-306586203093030 TABLET in 1 BOTTLE (65862-309-30)
65862-309-99658620309991000 TABLET in 1 BOTTLE (65862-309-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/35019655-9a30-4305-a262-936ad0e73071

  • NADAC price for package 65862030901

    GET /v1/drugs/nadac/65862030901

Use it

Look up 65862-309 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-309 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-309. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.