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Diltiazem Hydrochloride

NDC 62332-782, Diltiazem Hydrochloride, tablet, film coated, from Alembic Pharmaceuticals Inc..

Product NDC
62332-782
Status
Listed
Labeler
Alembic Pharmaceuticals Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217633
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62332-782 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DILTIAZEM HYDROCHLORIDE60 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
62332-782-3162332078231100 TABLET, FILM COATED in 1 BOTTLE (62332-782-31)
62332-782-7162332078271500 TABLET, FILM COATED in 1 BOTTLE (62332-782-71)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ab38794a-914d-4bcd-9c6d-1578aa10041a

  • NADAC price for package 62332078231

    GET /v1/drugs/nadac/62332078231

Use it

Look up 62332-782 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62332-782 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62332-782. 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.