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Diltiazem Hydrochloride

NDC 71335-0579, Diltiazem Hydrochloride, tablet, from Bryant Ranch Prepack.

Product NDC
71335-0579
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA018602
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0579 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DILTIAZEM HYDROCHLORIDE90 mg/1

Pharmacologic classes

Calcium Channel Antagonists [MoA]; Calcium Channel Blocker [EPC]; Cytochrome P450 3A4 Inhibitors [MoA]

Package NDCNDC-11Package
71335-0579-17133505790130 TABLET in 1 BOTTLE (71335-0579-1)
71335-0579-27133505790290 TABLET in 1 BOTTLE (71335-0579-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/225a87fb-d353-4ee7-bd08-14d631ff6b16

Use it

Look up 71335-0579 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0579 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-0579. 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.