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Diltiazem hydrochloride

NDC 63304-722, Diltiazem hydrochloride, capsule, extended release, from Sun Pharmaceutical Industries, Inc..

Product NDC
63304-722
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203023
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63304-722 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DILTIAZEM HYDROCHLORIDE360 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
63304-722-0563304072205500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63304-722-05)
63304-722-306330407223030 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63304-722-30)
63304-722-906330407229090 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63304-722-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/976d9dd0-4f11-4439-b84e-0c0f0e018d8b

Use it

Look up 63304-722 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63304-722 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63304-722. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.