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Amlodipine Besylate

NDC 70518-1971, Amlodipine besylate, tablet, from REMEDYREPACK INC..

Product NDC
70518-1971
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078925
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-1971 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AMLODIPINE BESYLATE2.5 mg/1

Pharmacologic classes

Calcium Channel Antagonists [MoA]; Calcium Channel Blocker [EPC]; Cytochrome P450 3A Inhibitors [MoA]; Dihydropyridine Calcium Channel Blocker [EPC]; Dihydropyridines [CS]

Package NDCNDC-11Package
70518-1971-07051819710030 TABLET in 1 BLISTER PACK (70518-1971-0)
70518-1971-17051819710190 TABLET in 1 BOTTLE, PLASTIC (70518-1971-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4ad016ec-e158-4325-9f45-4460cf78dd98

Use it

Look up 70518-1971 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-1971 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-1971. 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.