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Diltiazem Hydrochloride

NDC 51655-020, Diltiazem Hydrochloride, tablet, film coated, from Northwind Health Company, LLC.

Product NDC
51655-020
Status
Listed
Labeler
Northwind Health Company, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA074185
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51655-020 \
  -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
51655-020-525165500205230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-020-52)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f29febd6-5a27-eb83-e053-2a95a90a5b7d

Use it

Look up 51655-020 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51655-020 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51655-020. 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.