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Diltiazem Hydrochloride

NDC 27808-322, Diltiazem Hydrochloride, capsule, extended release, from Cranbury Pharmaceuticals, LLC.

Product NDC
27808-322
Status
Listed
Labeler
Cranbury Pharmaceuticals, LLC
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA219073
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/27808-322 \
  -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
27808-322-0127808032201100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (27808-322-01)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2ef6b112-d3e9-4999-a8e0-46fb40d1ad81

Use it

Look up 27808-322 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/27808-322 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 27808-322. 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.