United States · FDA National Drug Code directory
Felodipine
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 72162-1160_ed9ee5b6-5cf9-45bb-b321-74c902baf333
- Product NDC
- 72162-1160
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- Felodipine
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20111215
- Source listing expiry
- 20261231
Source-listed ingredients
- FELODIPINE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1160-1) · 72162-1160-1
- 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1160-5) · 72162-1160-5
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →