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Felodipine

NDC 65862-675, Felodipine, tablet, film coated, extended release, from Aurobindo Pharma Limited.

Product NDC
65862-675
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203417
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65862-675 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FELODIPINE10 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
65862-675-0165862067501100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-675-01)
65862-675-786586206757810 BLISTER PACK in 1 CARTON (65862-675-78) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (65862-675-10)
65862-675-906586206759090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-675-90)
65862-675-99658620675991000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-675-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dd39c559-5c5d-4d3b-9228-c44085e1699f

Use it

Look up 65862-675 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-675 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-675. 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.