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Diltiazem Hydrochloride

NDC 71335-2129, Diltiazem hydrochloride, capsule, extended release, from Bryant Ranch Prepack.

Product NDC
71335-2129
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205231
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2129 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DILTIAZEM HYDROCHLORIDE120 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
71335-2129-17133521290130 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2129-1)
71335-2129-27133521290290 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-2129-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/22e653e5-4122-4d7d-b9ad-0bdc1390fb40

Use it

Look up 71335-2129 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2129 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-2129. 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.