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Amlodipine Besylate

NDC 69097-836, Amlodipine Besylate, tablet, from Cipla USA Inc..

Product NDC
69097-836
Status
Listed
Labeler
Cipla USA Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077955
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69097-836 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AMLODIPINE BESYLATE2.5 mg/1

Pharmacologic classes

Calcium Channel Antagonists [MoA]; Dihydropyridine Calcium Channel Blocker [EPC]; Dihydropyridines [CS]

Package NDCNDC-11Package
69097-836-056909708360590 TABLET in 1 BOTTLE (69097-836-05)
69097-836-15690970836151000 TABLET in 1 BOTTLE (69097-836-15)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0c8d6b2f-3e4a-47a2-80e2-a34dcb337555

Use it

Look up 69097-836 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69097-836 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69097-836. 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.