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verapamil hydrochloride

NDC 70518-0605, verapamil hydrochloride, tablet, film coated, extended release, from REMEDYREPACK INC..

Product NDC
70518-0605
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090700
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-0605 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VERAPAMIL HYDROCHLORIDE180 mg/1

Pharmacologic classes

Calcium Channel Antagonists [MoA]; Calcium Channel Blocker [EPC]; Cytochrome P450 3A Inhibitors [MoA]; Cytochrome P450 3A4 Inhibitors [MoA]; P-Glycoprotein Inhibitors [MoA]

Package NDCNDC-11Package
70518-0605-27051806050250 POUCH in 1 BOX (70518-0605-2) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 POUCH (70518-0605-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ce9ab27a-e03b-4e40-a0e0-b586cd75dead

Use it

Look up 70518-0605 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-0605 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-0605. 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.