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Diltiazem Hydrochloride

NDC 70436-197, Diltiazem Hydrochloride, tablet, extended release, from Slate Run Pharmaceuticals, LLC.

Product NDC
70436-197
Status
Listed
Labeler
Slate Run Pharmaceuticals, LLC
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216439
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70436-197 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DILTIAZEM HYDROCHLORIDE240 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
70436-197-047043601970430 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-197-04)
70436-197-067043601970690 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-197-06)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f7137458-0db3-7ecd-e053-6394a90a5f95

  • NADAC price for package 70436019704

    GET /v1/drugs/nadac/70436019704

Use it

Look up 70436-197 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70436-197 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70436-197. 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.