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Diltiazem Hydrochloride

NDC 68462-851, Diltiazem Hydrochloride, capsule, extended release, from GLENMARK PHARMACEUTICALS INC., USA.

Product NDC
68462-851
Status
Listed
Labeler
GLENMARK PHARMACEUTICALS INC., USA
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212317
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68462-851 \
  -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
68462-851-0168462085101100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68462-851-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fb1606ea-1cff-46fd-b8e5-8135da76436c

  • NADAC price for package 68462085101

    GET /v1/drugs/nadac/68462085101

Use it

Look up 68462-851 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68462-851 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68462-851. 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.