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Diltiazem Hydrochloride

NDC 68682-008, Diltiazem Hydrochloride, tablet, from Oceanside Pharmaceuticals.

Product NDC
68682-008
Status
Listed
Labeler
Oceanside Pharmaceuticals
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/68682-008 \
  -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]

Package NDCNDC-11Package
68682-008-1068682000810100 TABLET in 1 BOTTLE (68682-008-10)
68682-008-5068682000850500 TABLET in 1 BOTTLE (68682-008-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f6a24de7-8ffe-48af-873f-10fdcd5551d1

Use it

Look up 68682-008 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68682-008 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68682-008. 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.