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AMLODIPINE BESYLATE

NDC 51655-869, AMLODIPINE BESYLATE, tablet, from Northwind Health Company, LLC.

Product NDC
51655-869
Status
Listed
Labeler
Northwind Health Company, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077073
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51655-869 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • AMLODIPINE BESYLATE10 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
51655-869-265165508692690 TABLET in 1 BOTTLE, PLASTIC (51655-869-26)
51655-869-525165508695230 TABLET in 1 BOTTLE, PLASTIC (51655-869-52)
51655-869-8351655086983180 TABLET in 1 BOTTLE, PLASTIC (51655-869-83)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/03fe9ad2-3a1a-78db-e063-6294a90a2ed3

Use it

Look up 51655-869 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51655-869 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51655-869. 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.