United States · FDA National Drug Code directory
ZYPITAMAG
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
- 25208-202_d39ef44a-4e4d-459d-86bd-79394202e3ec
- Product NDC
- 25208-202
- Form
- TABLET, FILM COATED
- Composition / generic term
- Pitavastatin Magnesium
- Labeler
- Medicure International Inc
- Marketing category
- NDA
- Marketing start / end (source format)
- 20180309
- Source listing expiry
- 20261231
Source-listed ingredients
- PITAVASTATIN — 4 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 TABLET, FILM COATED in 1 BOTTLE (25208-202-09) · 25208-202-09
- 500 TABLET, FILM COATED in 1 BOTTLE (25208-202-15) · 25208-202-15
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 →