United States · FDA National Drug Code directory

METOPROLOL TARTRATE

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
71205-003_27fbee5a-d8d4-4c8a-853a-95f6f61bc4a5
Product NDC
71205-003
Form
TABLET
Composition / generic term
METOPROLOL
Labeler
Proficient Rx LP
Marketing category
ANDA
Marketing start / end (source format)
20160731
Source listing expiry
20271231

Source-listed ingredients

  • METOPROLOL TARTRATE — 25 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BOTTLE (71205-003-30) · 71205-003-30
  • 60 TABLET in 1 BOTTLE (71205-003-60) · 71205-003-60
  • 180 TABLET in 1 BOTTLE (71205-003-78) · 71205-003-78
  • 90 TABLET in 1 BOTTLE (71205-003-90) · 71205-003-90

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.

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METOPROLOL TARTRATE — United States | Molindra Medicines