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Diltiazem Hydrochloride

NDC 71335-3135, Diltiazem Hydrochloride, tablet, from Bryant Ranch Prepack.

Product NDC
71335-3135
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216521
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-3135 \
  -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
71335-3135-17133531350130 TABLET in 1 BOTTLE (71335-3135-1)
71335-3135-27133531350290 TABLET in 1 BOTTLE (71335-3135-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/50df9f09-aa2f-495d-a25c-7c5c0fdffcf0

Use it

Look up 71335-3135 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-3135 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-3135. 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.