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Diltiazem hydrochloride

NDC 72578-199, Diltiazem hydrochloride, tablet, from Viona Pharmaceuticals Inc.

Product NDC
72578-199
Status
Listed
Labeler
Viona Pharmaceuticals Inc
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA219253
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72578-199 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DILTIAZEM HYDROCHLORIDE30 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72578-199-0172578019901100 TABLET in 1 BOTTLE (72578-199-01)
72578-199-0572578019905500 TABLET in 1 BOTTLE (72578-199-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/43cffe12-304a-4e15-9512-94f812188f1a

Use it

Look up 72578-199 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72578-199 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72578-199. 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.